CARD8 (caspase recruitment domain family member 8) - Rat Genome Database

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Gene: CARD8 (caspase recruitment domain family member 8) Homo sapiens
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Symbol: CARD8
Name: caspase recruitment domain family member 8
RGD ID: 1351599
HGNC Page HGNC:17057
Description: Enables several functions, including molecular condensate scaffold activity; peptidase activator activity; and protein domain specific binding activity. Involved in several processes, including negative regulation of signal transduction; protein-containing complex assembly; and regulation of interleukin-1 beta production. Located in nucleoplasm. Part of NLRP3 inflammasome complex. Is active in CARD8 inflammasome complex. Implicated in inflammatory bowel disease 30.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: apoptotic protein NDPP1; CARD inhibitor of NF-kappaB-activating ligands; CARDINAL; caspase recruitment domain family, member 8; caspase recruitment domain-containing protein 8; DACAR; Dakar; DKFZp779L0366; FLJ18119; FLJ18121; KIAA0955; MGC57162; NDPP; NDPP1; TUCAN; tumor up-regulated CARD-containing antagonist of CASP9; tumor up-regulated CARD-containing antagonist of caspase nine
RGD Orthologs
Bonobo
Dog
Green Monkey
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381948,179,825 - 48,255,946 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1948,180,770 - 48,255,946 (-)EnsemblGRCh38hg38GRCh38
GRCh371948,706,405 - 48,759,203 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361953,403,325 - 53,444,737 (-)NCBINCBI36Build 36hg18NCBI36
Build 341953,403,324 - 53,444,734NCBI
Celera1945,576,569 - 45,624,446 (-)NCBICelera
Cytogenetic Map19q13.33NCBI
HuRef1945,093,304 - 45,141,176 (-)NCBIHuRef
CHM1_11948,713,493 - 48,761,345 (-)NCBICHM1_1
T2T-CHM13v2.01951,197,212 - 51,250,053 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. Immunological and inflammatory functions of the interleukin-1 family. Dinarello CA Annu Rev Immunol. 2009;27:519-50.
2. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
3. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:10231032   PMID:11408476   PMID:11551959   PMID:11821383   PMID:11956601   PMID:12067710   PMID:12107410   PMID:12477932   PMID:12775719   PMID:14702039   PMID:15030775   PMID:15489334  
PMID:16344560   PMID:16712791   PMID:16796750   PMID:17030188   PMID:17484912   PMID:17595233   PMID:17878386   PMID:18092344   PMID:18212821   PMID:18263599   PMID:18311798   PMID:18841008  
PMID:19074885   PMID:19252766   PMID:19319132   PMID:19322201   PMID:19443463   PMID:19664744   PMID:19843337   PMID:19940360   PMID:20182451   PMID:20379614   PMID:20385562   PMID:20453000  
PMID:20800603   PMID:21248762   PMID:21308686   PMID:21621776   PMID:21873635   PMID:22087307   PMID:22128899   PMID:22199357   PMID:22227487   PMID:23053059   PMID:23088220   PMID:23506543  
PMID:23507658   PMID:23547871   PMID:23563199   PMID:23611467   PMID:23695559   PMID:24098386   PMID:24385277   PMID:24517500   PMID:25564880   PMID:25790751   PMID:25895569   PMID:25921775  
PMID:26095808   PMID:26186194   PMID:26283210   PMID:26462562   PMID:26462578   PMID:27110561   PMID:27550484   PMID:27810076   PMID:28135700   PMID:28137891   PMID:28185410   PMID:28514442  
PMID:28718761   PMID:29097263   PMID:29230505   PMID:29408806   PMID:30088494   PMID:30211233   PMID:30816317   PMID:31525884   PMID:31529732   PMID:32080163   PMID:32104685   PMID:32396255  
PMID:32613553   PMID:32689633   PMID:32840892   PMID:33053349   PMID:33067783   PMID:33154409   PMID:33164551   PMID:33420028   PMID:33420033   PMID:33542150   PMID:33961781   PMID:34019797  
PMID:34587665   PMID:35580636   PMID:36649710   PMID:36649711   PMID:36835594   PMID:36870425   PMID:36931259   PMID:37276232   PMID:37311351   PMID:37417868   PMID:37712526   PMID:38350853  


Genomics

Comparative Map Data
CARD8
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381948,179,825 - 48,255,946 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1948,180,770 - 48,255,946 (-)EnsemblGRCh38hg38GRCh38
GRCh371948,706,405 - 48,759,203 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361953,403,325 - 53,444,737 (-)NCBINCBI36Build 36hg18NCBI36
Build 341953,403,324 - 53,444,734NCBI
Celera1945,576,569 - 45,624,446 (-)NCBICelera
Cytogenetic Map19q13.33NCBI
HuRef1945,093,304 - 45,141,176 (-)NCBIHuRef
CHM1_11948,713,493 - 48,761,345 (-)NCBICHM1_1
T2T-CHM13v2.01951,197,212 - 51,250,053 (-)NCBIT2T-CHM13v2.0
CARD8
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22054,308,114 - 54,360,131 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11956,234,309 - 56,286,412 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01945,204,735 - 45,256,481 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11953,798,913 - 53,850,328 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1953,798,967 - 53,850,328 (-)Ensemblpanpan1.1panPan2
LOC491519
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11107,994,215 - 108,025,875 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1107,507,437 - 107,519,633 (+)NCBIDog10K_Boxer_Tasha
LOC103234962
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1641,446,890 - 41,500,098 (-)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366607321,233,430 - 21,247,488 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in CARD8
317 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19q13.32-13.33(chr19:46658791-49050450)x3 copy number gain See cases [RCV000052913] Chr19:46658791..49050450 [GRCh38]
Chr19:47162048..49553707 [GRCh37]
Chr19:51853888..54245519 [NCBI36]
Chr19:19q13.32-13.33		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3 copy number gain See cases [RCV000052914] Chr19:47908540..58539965 [GRCh38]
Chr19:48411797..59051332 [GRCh37]
Chr19:53103609..63743144 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3 copy number gain See cases [RCV000052915] Chr19:47929575..58572206 [GRCh38]
Chr19:48432832..59083573 [GRCh37]
Chr19:53124644..63775385 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
NM_001184900.3(CARD8):c.391+5T>C single nucleotide variant not provided [RCV001348067] Chr19:48232448 [GRCh38]
Chr19:48735705 [GRCh37]
Chr19:19q13.33		 uncertain significance
GRCh38/hg38 19q13.32-13.33(chr19:44971420-48257402)x3 copy number gain See cases [RCV000136578] Chr19:44971420..48257402 [GRCh38]
Chr19:45474677..48760659 [GRCh37]
Chr19:50166517..53452471 [NCBI36]
Chr19:19q13.32-13.33		 pathogenic
NM_001184900.3(CARD8):c.130G>A (p.Val44Ile) single nucleotide variant Inflammatory bowel disease 30 [RCV001263446]|not specified [RCV000238764] Chr19:48238462 [GRCh38]
Chr19:48741719 [GRCh37]
Chr19:19q13.33		 pathogenic|uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic|uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 copy number gain not provided [RCV000752439] Chr19:68029..59110290 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 copy number gain not provided [RCV000752444] Chr19:260912..59097160 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19q13.33(chr19:48740358-48764857)x3 copy number gain not provided [RCV000740195] Chr19:48740358..48764857 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.693C>T (p.Gly231=) single nucleotide variant not provided [RCV000926239] Chr19:48230856 [GRCh38]
Chr19:48734113 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1017C>T (p.Ser339=) single nucleotide variant not provided [RCV000920716] Chr19:48230456 [GRCh38]
Chr19:48733713 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.592G>A (p.Gly198Ser) single nucleotide variant not provided [RCV000964390] Chr19:48230957 [GRCh38]
Chr19:48734214 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.1416C>T (p.Leu472=) single nucleotide variant not provided [RCV000964072] Chr19:48211908 [GRCh38]
Chr19:48715165 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.1086G>A (p.Ser362=) single nucleotide variant not provided [RCV000878994] Chr19:48221805 [GRCh38]
Chr19:48725062 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.916G>A (p.Ala306Thr) single nucleotide variant CARD8-related condition [RCV003970712]|Inborn genetic diseases [RCV002547206]|not provided [RCV000950491] Chr19:48230557 [GRCh38]
Chr19:48733814 [GRCh37]
Chr19:19q13.33		 likely benign|uncertain significance
GRCh37/hg19 19q13.33(chr19:48119589-49595956)x3 copy number gain not provided [RCV000848800] Chr19:48119589..49595956 [GRCh37]
Chr19:19q13.33		 uncertain significance
GRCh37/hg19 19q13.31-13.42(chr19:44738088-53621561)x3 copy number gain not provided [RCV001007050] Chr19:44738088..53621561 [GRCh37]
Chr19:19q13.31-13.42		 pathogenic
GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3 copy number gain not provided [RCV000845733] Chr19:28271106..49213832 [GRCh37]
Chr19:19q11-13.33		 pathogenic
NM_001184900.3(CARD8):c.1009G>T (p.Val337Phe) single nucleotide variant not provided [RCV003104447] Chr19:48230464 [GRCh38]
Chr19:48733721 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.210G>A (p.Thr70=) single nucleotide variant not provided [RCV001907911] Chr19:48234543 [GRCh38]
Chr19:48737800 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.743T>G (p.Ile248Ser) single nucleotide variant Inborn genetic diseases [RCV003242025]|not provided [RCV003730498] Chr19:48230806 [GRCh38]
Chr19:48734063 [GRCh37]
Chr19:19q13.33		 uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:48463931-57095254)x3 copy number gain not provided [RCV001259944] Chr19:48463931..57095254 [GRCh37]
Chr19:19q13.33-13.43		 pathogenic
NM_001184900.3(CARD8):c.970C>T (p.His324Tyr) single nucleotide variant CARD8-related condition [RCV003426050]|Inborn genetic diseases [RCV002546885]|not provided [RCV001339873] Chr19:48230503 [GRCh38]
Chr19:48733760 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.480G>C (p.Gln160His) single nucleotide variant not provided [RCV001373736] Chr19:48231722 [GRCh38]
Chr19:48734979 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1245A>T (p.Gln415His) single nucleotide variant not provided [RCV001295285] Chr19:48218929 [GRCh38]
Chr19:48722186 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.11dup (p.Glu5fs) duplication not provided [RCV001306034] Chr19:48241009..48241010 [GRCh38]
Chr19:48744266..48744267 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.536dup (p.Tyr180fs) duplication not provided [RCV001300860] Chr19:48231665..48231666 [GRCh38]
Chr19:48734922..48734923 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.544G>T (p.Val182Phe) single nucleotide variant not provided [RCV001396206] Chr19:48231005 [GRCh38]
Chr19:48734262 [GRCh37]
Chr19:19q13.33		 likely benign
NC_000019.9:g.(?_48714967)_(48737820_?)del deletion not provided [RCV001316314] Chr19:48714967..48737820 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.246T>C (p.Leu82=) single nucleotide variant not provided [RCV001519350] Chr19:48234507 [GRCh38]
Chr19:48737764 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.623C>T (p.Thr208Met) single nucleotide variant CARD8-related condition [RCV003946236]|not provided [RCV001475970] Chr19:48230926 [GRCh38]
Chr19:48734183 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.304T>A (p.Phe102Ile) single nucleotide variant not provided [RCV001514794] Chr19:48234449 [GRCh38]
Chr19:48737706 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.53C>T (p.Pro18Leu) single nucleotide variant CARD8-related condition [RCV003940869]|not provided [RCV001500083] Chr19:48240968 [GRCh38]
Chr19:48744225 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.611A>C (p.Glu204Ala) single nucleotide variant not provided [RCV001515023] Chr19:48230938 [GRCh38]
Chr19:48734195 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.517A>G (p.Ile173Val) single nucleotide variant not provided [RCV001515024] Chr19:48231685 [GRCh38]
Chr19:48734942 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.1385A>G (p.Gln462Arg) single nucleotide variant not provided [RCV001520215] Chr19:48211939 [GRCh38]
Chr19:48715196 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.260A>C (p.His87Pro) single nucleotide variant not provided [RCV001512283] Chr19:48234493 [GRCh38]
Chr19:48737750 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.1157C>T (p.Pro386Leu) single nucleotide variant CARD8-related condition [RCV003938867]|not provided [RCV001484252] Chr19:48221734 [GRCh38]
Chr19:48724991 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1549C>G (p.Leu517Val) single nucleotide variant not provided [RCV001444402] Chr19:48211775 [GRCh38]
Chr19:48715032 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1545C>T (p.Asp515=) single nucleotide variant not provided [RCV001519347] Chr19:48211779 [GRCh38]
Chr19:48715036 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.1428A>G (p.Gln476=) single nucleotide variant not provided [RCV001519348] Chr19:48211896 [GRCh38]
Chr19:48715153 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.1251G>A (p.Glu417=) single nucleotide variant not provided [RCV001519349] Chr19:48218923 [GRCh38]
Chr19:48722180 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.772+16C>T single nucleotide variant not provided [RCV001515680] Chr19:48230761 [GRCh38]
Chr19:48734018 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.210-12G>C single nucleotide variant not provided [RCV001512375] Chr19:48234555 [GRCh38]
Chr19:48737812 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.1066G>C (p.Gly356Arg) single nucleotide variant not provided [RCV001513490] Chr19:48221825 [GRCh38]
Chr19:48725082 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.1162-18C>T single nucleotide variant not provided [RCV001519582] Chr19:48219030 [GRCh38]
Chr19:48722287 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.974C>G (p.Pro325Arg) single nucleotide variant not provided [RCV001515021] Chr19:48230499 [GRCh38]
Chr19:48733756 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.867T>C (p.Ala289=) single nucleotide variant not provided [RCV001515022] Chr19:48230606 [GRCh38]
Chr19:48733863 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.654G>C (p.Leu218=) single nucleotide variant not provided [RCV001463844] Chr19:48230895 [GRCh38]
Chr19:48734152 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.440_441dup (p.Val148fs) duplication not provided [RCV001522653] Chr19:48231760..48231761 [GRCh38]
Chr19:48735017..48735018 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.1483C>T (p.Arg495Trp) single nucleotide variant not provided [RCV001950019] Chr19:48211841 [GRCh38]
Chr19:48715098 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.308G>A (p.Arg103His) single nucleotide variant not provided [RCV001949713] Chr19:48234445 [GRCh38]
Chr19:48737702 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1094T>G (p.Met365Arg) single nucleotide variant Inborn genetic diseases [RCV002553623]|not provided [RCV001896117] Chr19:48221797 [GRCh38]
Chr19:48725054 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1058G>A (p.Arg353His) single nucleotide variant not provided [RCV001929356] Chr19:48221833 [GRCh38]
Chr19:48725090 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.307C>T (p.Arg103Cys) single nucleotide variant not provided [RCV001928738] Chr19:48234446 [GRCh38]
Chr19:48737703 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.815A>G (p.Lys272Arg) single nucleotide variant not provided [RCV002022382] Chr19:48230658 [GRCh38]
Chr19:48733915 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.676G>C (p.Glu226Gln) single nucleotide variant not provided [RCV002009018] Chr19:48230873 [GRCh38]
Chr19:48734130 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.302T>G (p.Leu101Trp) single nucleotide variant not provided [RCV001893761] Chr19:48234451 [GRCh38]
Chr19:48737708 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.953A>G (p.Asn318Ser) single nucleotide variant not provided [RCV002023199] Chr19:48230520 [GRCh38]
Chr19:48733777 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1585G>A (p.Val529Met) single nucleotide variant not provided [RCV002020932] Chr19:48211739 [GRCh38]
Chr19:48714996 [GRCh37]
Chr19:19q13.33		 uncertain significance
NC_000019.9:g.(?_48337701)_(48725132_?)dup duplication Leber congenital amaurosis 7 [RCV002004465] Chr19:48337701..48725132 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.352G>C (p.Val118Leu) single nucleotide variant CARD8-related condition [RCV003401839]|Inborn genetic diseases [RCV002553598]|not provided [RCV001910901] Chr19:48232492 [GRCh38]
Chr19:48735749 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1161+5G>A single nucleotide variant not provided [RCV002003406] Chr19:48221725 [GRCh38]
Chr19:48724982 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.276TGA[1] (p.Asp93del) microsatellite not provided [RCV001968667] Chr19:48234472..48234474 [GRCh38]
Chr19:48737729..48737731 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.853G>T (p.Glu285Ter) single nucleotide variant Inflammatory bowel disease 30 [RCV003138048]|not provided [RCV002023623] Chr19:48230620 [GRCh38]
Chr19:48733877 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1484G>A (p.Arg495Gln) single nucleotide variant Inborn genetic diseases [RCV002554369]|not provided [RCV001913243] Chr19:48211840 [GRCh38]
Chr19:48715097 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1375C>T (p.Arg459Trp) single nucleotide variant Inborn genetic diseases [RCV002563459]|not provided [RCV001985483] Chr19:48211949 [GRCh38]
Chr19:48715206 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.802G>A (p.Val268Ile) single nucleotide variant Inborn genetic diseases [RCV002557826]|not provided [RCV001910566] Chr19:48230671 [GRCh38]
Chr19:48733928 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1035+5G>A single nucleotide variant not provided [RCV002044444] Chr19:48230433 [GRCh38]
Chr19:48733690 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.973C>A (p.Pro325Thr) single nucleotide variant CARD8-related condition [RCV003923356]|Inborn genetic diseases [RCV002555647]|not provided [RCV001908992] Chr19:48230500 [GRCh38]
Chr19:48733757 [GRCh37]
Chr19:19q13.33		 likely benign|uncertain significance
NM_001184900.3(CARD8):c.1303+2T>G single nucleotide variant not provided [RCV001965451] Chr19:48218869 [GRCh38]
Chr19:48722126 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.754C>G (p.His252Asp) single nucleotide variant not provided [RCV002021386] Chr19:48230795 [GRCh38]
Chr19:48734052 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.491C>G (p.Pro164Arg) single nucleotide variant not provided [RCV002020859] Chr19:48231711 [GRCh38]
Chr19:48734968 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.414T>A (p.Asn138Lys) single nucleotide variant not provided [RCV002037158] Chr19:48231788 [GRCh38]
Chr19:48735045 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.215A>G (p.Tyr72Cys) single nucleotide variant not provided [RCV001957863] Chr19:48234538 [GRCh38]
Chr19:48737795 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.754C>T (p.His252Tyr) single nucleotide variant not provided [RCV001975792] Chr19:48230795 [GRCh38]
Chr19:48734052 [GRCh37]
Chr19:19q13.33		 uncertain significance
NC_000019.9:g.(?_48714967)_(48725132_?)del deletion not provided [RCV002018394] Chr19:48714967..48725132 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.3G>A (p.Met1Ile) single nucleotide variant not provided [RCV001924663] Chr19:48241018 [GRCh38]
Chr19:48744275 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1324G>C (p.Ala442Pro) single nucleotide variant Inborn genetic diseases [RCV002557841]|not provided [RCV001943432] Chr19:48215364 [GRCh38]
Chr19:48718621 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.232G>A (p.Val78Ile) single nucleotide variant not provided [RCV001962691] Chr19:48234521 [GRCh38]
Chr19:48737778 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.543-9T>A single nucleotide variant not provided [RCV001881351] Chr19:48231015 [GRCh38]
Chr19:48734272 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.24A>T (p.Glu8Asp) single nucleotide variant not provided [RCV001942557] Chr19:48240997 [GRCh38]
Chr19:48744254 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1093A>G (p.Met365Val) single nucleotide variant not provided [RCV001943604] Chr19:48221798 [GRCh38]
Chr19:48725055 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.2T>C (p.Met1Thr) single nucleotide variant not provided [RCV001885883] Chr19:48241019 [GRCh38]
Chr19:48744276 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.542G>A (p.Ser181Asn) single nucleotide variant not provided [RCV001921172] Chr19:48231660 [GRCh38]
Chr19:48734917 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.284C>T (p.Thr95Ile) single nucleotide variant not provided [RCV002014203] Chr19:48234469 [GRCh38]
Chr19:48737726 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.308G>T (p.Arg103Leu) single nucleotide variant not provided [RCV001936346] Chr19:48234445 [GRCh38]
Chr19:48737702 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1057C>G (p.Arg353Gly) single nucleotide variant not provided [RCV002046896] Chr19:48221834 [GRCh38]
Chr19:48725091 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.497G>C (p.Gly166Ala) single nucleotide variant not provided [RCV001876518] Chr19:48231705 [GRCh38]
Chr19:48734962 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.336G>T (p.Gly112=) single nucleotide variant not provided [RCV001864961] Chr19:48234417 [GRCh38]
Chr19:48737674 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.755A>G (p.His252Arg) single nucleotide variant Inborn genetic diseases [RCV002557707]|not provided [RCV001933200] Chr19:48230794 [GRCh38]
Chr19:48734051 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.999del (p.Leu334fs) deletion not provided [RCV002014815] Chr19:48230474 [GRCh38]
Chr19:48733731 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1017C>A (p.Ser339Arg) single nucleotide variant not provided [RCV001958103] Chr19:48230456 [GRCh38]
Chr19:48733713 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1149A>G (p.Lys383=) single nucleotide variant not provided [RCV001867012] Chr19:48221742 [GRCh38]
Chr19:48724999 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1440_1443dup (p.Thr482fs) duplication not provided [RCV001938370] Chr19:48211880..48211881 [GRCh38]
Chr19:48715137..48715138 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1276T>A (p.Leu426Met) single nucleotide variant not provided [RCV001978569] Chr19:48218898 [GRCh38]
Chr19:48722155 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.838C>T (p.His280Tyr) single nucleotide variant not provided [RCV001936133] Chr19:48230635 [GRCh38]
Chr19:48733892 [GRCh37]
Chr19:19q13.33		 uncertain significance
NC_000019.9:g.(?_48724967)_(48725132_?)del deletion not provided [RCV001982450] Chr19:48724967..48725132 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.543-12G>A single nucleotide variant not provided [RCV001938607] Chr19:48231018 [GRCh38]
Chr19:48734275 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.335G>C (p.Gly112Ala) single nucleotide variant not provided [RCV002035126] Chr19:48234418 [GRCh38]
Chr19:48737675 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.273del (p.Asp92fs) deletion not provided [RCV001925335] Chr19:48234480 [GRCh38]
Chr19:48737737 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.509T>C (p.Val170Ala) single nucleotide variant not provided [RCV001879436] Chr19:48231693 [GRCh38]
Chr19:48734950 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.679C>G (p.Gln227Glu) single nucleotide variant not provided [RCV001901188] Chr19:48230870 [GRCh38]
Chr19:48734127 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.382C>T (p.Gln128Ter) single nucleotide variant not provided [RCV001938213] Chr19:48232462 [GRCh38]
Chr19:48735719 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1021G>A (p.Ala341Thr) single nucleotide variant not provided [RCV001961268] Chr19:48230452 [GRCh38]
Chr19:48733709 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.826A>C (p.Met276Leu) single nucleotide variant Inborn genetic diseases [RCV002548798]|not provided [RCV002018636] Chr19:48230647 [GRCh38]
Chr19:48733904 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.342C>A (p.Asp114Glu) single nucleotide variant not provided [RCV002029165] Chr19:48234411 [GRCh38]
Chr19:48737668 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.897G>A (p.Met299Ile) single nucleotide variant not provided [RCV002027953] Chr19:48230576 [GRCh38]
Chr19:48733833 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.599T>C (p.Leu200Pro) single nucleotide variant not provided [RCV001897919] Chr19:48230950 [GRCh38]
Chr19:48734207 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.754C>A (p.His252Asn) single nucleotide variant Inborn genetic diseases [RCV003247088]|not provided [RCV001902421] Chr19:48230795 [GRCh38]
Chr19:48734052 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1459_1460delinsTT (p.Glu487Leu) indel not provided [RCV001999016] Chr19:48211864..48211865 [GRCh38]
Chr19:48715121..48715122 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1018G>A (p.Asp340Asn) single nucleotide variant not provided [RCV001940719] Chr19:48230455 [GRCh38]
Chr19:48733712 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.856C>A (p.Pro286Thr) single nucleotide variant not provided [RCV001905544] Chr19:48230617 [GRCh38]
Chr19:48733874 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.910C>T (p.Arg304Trp) single nucleotide variant not provided [RCV001937218] Chr19:48230563 [GRCh38]
Chr19:48733820 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.863A>G (p.Tyr288Cys) single nucleotide variant CARD8-related condition [RCV003407848]|not provided [RCV001904034] Chr19:48230610 [GRCh38]
Chr19:48733867 [GRCh37]
Chr19:19q13.33		 uncertain significance
NC_000019.9:g.(?_48744199)_(48744277_?)del deletion not provided [RCV001918932] Chr19:48744199..48744277 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.28A>C (p.Ser10Arg) single nucleotide variant not provided [RCV001932533] Chr19:48240993 [GRCh38]
Chr19:48744250 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.767_768delinsCT (p.Leu256Pro) indel not provided [RCV001917168] Chr19:48230781..48230782 [GRCh38]
Chr19:48734038..48734039 [GRCh37]
Chr19:19q13.33		 uncertain significance
NC_000019.9:g.(?_48618906)_(50921204_?)dup duplication Developmental and epileptic encephalopathy, 12 [RCV001939968]|not provided [RCV001916178] Chr19:48618906..50921204 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.58C>T (p.Arg20Trp) single nucleotide variant Inborn genetic diseases [RCV003289219]|not provided [RCV001916443] Chr19:48240963 [GRCh38]
Chr19:48744220 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.351-3_351-2insACCTCCCATGATAC insertion not provided [RCV002130447] Chr19:48232495..48232496 [GRCh38]
Chr19:48735752..48735753 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.978C>T (p.His326=) single nucleotide variant not provided [RCV002085764] Chr19:48230495 [GRCh38]
Chr19:48733752 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.513G>A (p.Glu171=) single nucleotide variant not provided [RCV002086056] Chr19:48231689 [GRCh38]
Chr19:48734946 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.933C>G (p.Leu311=) single nucleotide variant not provided [RCV002076135] Chr19:48230540 [GRCh38]
Chr19:48733797 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.981C>T (p.Pro327=) single nucleotide variant not provided [RCV002086597] Chr19:48230492 [GRCh38]
Chr19:48733749 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.1038G>A (p.Ala346=) single nucleotide variant not provided [RCV002089019] Chr19:48221853 [GRCh38]
Chr19:48725110 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.59+14C>T single nucleotide variant not provided [RCV002166204] Chr19:48240948 [GRCh38]
Chr19:48744205 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.624G>A (p.Thr208=) single nucleotide variant not provided [RCV002089688] Chr19:48230925 [GRCh38]
Chr19:48734182 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.300A>G (p.Leu100=) single nucleotide variant not provided [RCV002167554] Chr19:48234453 [GRCh38]
Chr19:48737710 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.252C>T (p.Asp84=) single nucleotide variant not provided [RCV002088635] Chr19:48234501 [GRCh38]
Chr19:48737758 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.773-15G>C single nucleotide variant not provided [RCV002192231] Chr19:48230715 [GRCh38]
Chr19:48733972 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.850G>A (p.Val284Met) single nucleotide variant not provided [RCV002191871] Chr19:48230623 [GRCh38]
Chr19:48733880 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.498A>C (p.Gly166=) single nucleotide variant not provided [RCV002071591] Chr19:48231704 [GRCh38]
Chr19:48734961 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.333T>G (p.Ser111=) single nucleotide variant not provided [RCV002092687] Chr19:48234420 [GRCh38]
Chr19:48737677 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1304-14dup duplication not provided [RCV002114864] Chr19:48215397..48215398 [GRCh38]
Chr19:48718654..48718655 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1122T>C (p.Tyr374=) single nucleotide variant not provided [RCV002113792] Chr19:48221769 [GRCh38]
Chr19:48725026 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.772+8G>T single nucleotide variant not provided [RCV002112847] Chr19:48230769 [GRCh38]
Chr19:48734026 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1304-9C>T single nucleotide variant not provided [RCV002134113] Chr19:48215393 [GRCh38]
Chr19:48718650 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1162-13G>A single nucleotide variant not provided [RCV002092051] Chr19:48219025 [GRCh38]
Chr19:48722282 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1410G>C (p.Gly470=) single nucleotide variant not provided [RCV002151673] Chr19:48211914 [GRCh38]
Chr19:48715171 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.350+19T>C single nucleotide variant not provided [RCV002150491] Chr19:48234384 [GRCh38]
Chr19:48737641 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.327A>G (p.Gln109=) single nucleotide variant not provided [RCV002194331] Chr19:48234426 [GRCh38]
Chr19:48737683 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1304-19A>T single nucleotide variant not provided [RCV002197590] Chr19:48215403 [GRCh38]
Chr19:48718660 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.723A>G (p.Pro241=) single nucleotide variant not provided [RCV002077548] Chr19:48230826 [GRCh38]
Chr19:48734083 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1110T>C (p.Phe370=) single nucleotide variant not provided [RCV002094077] Chr19:48221781 [GRCh38]
Chr19:48725038 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.1227G>A (p.Gln409=) single nucleotide variant not provided [RCV002078581] Chr19:48218947 [GRCh38]
Chr19:48722204 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.354A>G (p.Val118=) single nucleotide variant not provided [RCV002134002] Chr19:48232490 [GRCh38]
Chr19:48735747 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1359T>C (p.Phe453=) single nucleotide variant not provided [RCV002197054] Chr19:48211965 [GRCh38]
Chr19:48715222 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.630G>A (p.Ala210=) single nucleotide variant not provided [RCV002179673] Chr19:48230919 [GRCh38]
Chr19:48734176 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.918C>T (p.Ala306=) single nucleotide variant not provided [RCV002178167] Chr19:48230555 [GRCh38]
Chr19:48733812 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1349-6A>G single nucleotide variant not provided [RCV002154007] Chr19:48211981 [GRCh38]
Chr19:48715238 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1164G>C (p.Glu388Asp) single nucleotide variant CARD8-related condition [RCV003951212]|not provided [RCV002121690] Chr19:48219010 [GRCh38]
Chr19:48722267 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1303+16A>C single nucleotide variant not provided [RCV002137887] Chr19:48218855 [GRCh38]
Chr19:48722112 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1161+1G>T single nucleotide variant not provided [RCV002120279] Chr19:48221729 [GRCh38]
Chr19:48724986 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1036-8T>C single nucleotide variant not provided [RCV002163961] Chr19:48221863 [GRCh38]
Chr19:48725120 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.773-7C>T single nucleotide variant not provided [RCV002164013] Chr19:48230707 [GRCh38]
Chr19:48733964 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.773-18G>A single nucleotide variant not provided [RCV002161091] Chr19:48230718 [GRCh38]
Chr19:48733975 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.210-12G>T single nucleotide variant not provided [RCV002137013] Chr19:48234555 [GRCh38]
Chr19:48737812 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.350+18G>A single nucleotide variant not provided [RCV002177456] Chr19:48234385 [GRCh38]
Chr19:48737642 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.351-19T>C single nucleotide variant not provided [RCV002161459] Chr19:48232512 [GRCh38]
Chr19:48735769 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1584C>T (p.Leu528=) single nucleotide variant not provided [RCV002161734] Chr19:48211740 [GRCh38]
Chr19:48714997 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.391+11A>G single nucleotide variant not provided [RCV002139865] Chr19:48232442 [GRCh38]
Chr19:48735699 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.903C>A (p.Ile301=) single nucleotide variant not provided [RCV002181500] Chr19:48230570 [GRCh38]
Chr19:48733827 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1303+14C>T single nucleotide variant not provided [RCV002204102] Chr19:48218857 [GRCh38]
Chr19:48722114 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.484C>T (p.Leu162=) single nucleotide variant not provided [RCV002143763] Chr19:48231718 [GRCh38]
Chr19:48734975 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1035+16T>G single nucleotide variant not provided [RCV002197911] Chr19:48230422 [GRCh38]
Chr19:48733679 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.915C>T (p.Ile305=) single nucleotide variant not provided [RCV002139166] Chr19:48230558 [GRCh38]
Chr19:48733815 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.801C>T (p.Leu267=) single nucleotide variant not provided [RCV002200068] Chr19:48230672 [GRCh38]
Chr19:48733929 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1303+15G>A single nucleotide variant not provided [RCV002161849] Chr19:48218856 [GRCh38]
Chr19:48722113 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.501T>C (p.Asn167=) single nucleotide variant not provided [RCV002138691] Chr19:48231701 [GRCh38]
Chr19:48734958 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.432T>C (p.Tyr144=) single nucleotide variant not provided [RCV002099684] Chr19:48231770 [GRCh38]
Chr19:48735027 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1496A>G (p.Asn499Ser) single nucleotide variant not provided [RCV003115416] Chr19:48211828 [GRCh38]
Chr19:48715085 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1085C>T (p.Ser362Leu) single nucleotide variant not provided [RCV003118760] Chr19:48221806 [GRCh38]
Chr19:48725063 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.391+1G>C single nucleotide variant not provided [RCV003121650] Chr19:48232452 [GRCh38]
Chr19:48735709 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.139A>G (p.Ser47Gly) single nucleotide variant Inflammatory bowel disease 30 [RCV002289074] Chr19:48238453 [GRCh38]
Chr19:48741710 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1318G>A (p.Val440Ile) single nucleotide variant not provided [RCV002303667] Chr19:48215370 [GRCh38]
Chr19:48718627 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1334C>T (p.Pro445Leu) single nucleotide variant not provided [RCV002975440] Chr19:48215354 [GRCh38]
Chr19:48718611 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.770A>G (p.Gln257Arg) single nucleotide variant not provided [RCV002794967] Chr19:48230779 [GRCh38]
Chr19:48734036 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1099C>A (p.Pro367Thr) single nucleotide variant not provided [RCV002837914] Chr19:48221792 [GRCh38]
Chr19:48725049 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1188T>C (p.Pro396=) single nucleotide variant not provided [RCV003032561] Chr19:48218986 [GRCh38]
Chr19:48722243 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1069G>T (p.Val357Leu) single nucleotide variant not provided [RCV002618547] Chr19:48221822 [GRCh38]
Chr19:48725079 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.595T>C (p.Phe199Leu) single nucleotide variant not provided [RCV002824902] Chr19:48230954 [GRCh38]
Chr19:48734211 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.911G>A (p.Arg304Gln) single nucleotide variant not provided [RCV002662781] Chr19:48230562 [GRCh38]
Chr19:48733819 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1062C>G (p.Phe354Leu) single nucleotide variant Inborn genetic diseases [RCV002784607]|not provided [RCV003778645] Chr19:48221829 [GRCh38]
Chr19:48725086 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1290T>C (p.Thr430=) single nucleotide variant not provided [RCV002871227] Chr19:48218884 [GRCh38]
Chr19:48722141 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.739G>A (p.Glu247Lys) single nucleotide variant not provided [RCV002740494] Chr19:48230810 [GRCh38]
Chr19:48734067 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1540C>T (p.Leu514=) single nucleotide variant not provided [RCV002740501] Chr19:48211784 [GRCh38]
Chr19:48715041 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.523A>G (p.Lys175Glu) single nucleotide variant not provided [RCV002825291] Chr19:48231679 [GRCh38]
Chr19:48734936 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.350+7A>G single nucleotide variant not provided [RCV002885947] Chr19:48234396 [GRCh38]
Chr19:48737653 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1256C>A (p.Thr419Asn) single nucleotide variant not provided [RCV003018384] Chr19:48218918 [GRCh38]
Chr19:48722175 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1075C>T (p.Leu359=) single nucleotide variant not provided [RCV002781204] Chr19:48221816 [GRCh38]
Chr19:48725073 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.396C>T (p.Asp132=) single nucleotide variant not provided [RCV002638407] Chr19:48231806 [GRCh38]
Chr19:48735063 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.350+1G>A single nucleotide variant not provided [RCV003053825] Chr19:48234402 [GRCh38]
Chr19:48737659 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1086G>T (p.Ser362=) single nucleotide variant not provided [RCV002621491] Chr19:48221805 [GRCh38]
Chr19:48725062 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1036-13C>T single nucleotide variant not provided [RCV002706770] Chr19:48221868 [GRCh38]
Chr19:48725125 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1367A>G (p.Glu456Gly) single nucleotide variant Inborn genetic diseases [RCV002924373] Chr19:48211957 [GRCh38]
Chr19:48715214 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.928C>T (p.Arg310Cys) single nucleotide variant not provided [RCV002979656] Chr19:48230545 [GRCh38]
Chr19:48733802 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.544G>A (p.Val182Ile) single nucleotide variant not provided [RCV002570096] Chr19:48231005 [GRCh38]
Chr19:48734262 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.160A>G (p.Thr54Ala) single nucleotide variant Inborn genetic diseases [RCV002781632] Chr19:48238432 [GRCh38]
Chr19:48741689 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1545C>G (p.Asp515Glu) single nucleotide variant not provided [RCV003080779] Chr19:48211779 [GRCh38]
Chr19:48715036 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.379G>C (p.Gly127Arg) single nucleotide variant not provided [RCV002948946] Chr19:48232465 [GRCh38]
Chr19:48735722 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1072C>T (p.Arg358Cys) single nucleotide variant not provided [RCV002596120] Chr19:48221819 [GRCh38]
Chr19:48725076 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.737C>T (p.Ala246Val) single nucleotide variant not provided [RCV002643105] Chr19:48230812 [GRCh38]
Chr19:48734069 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.220G>A (p.Glu74Lys) single nucleotide variant not provided [RCV002645670] Chr19:48234533 [GRCh38]
Chr19:48737790 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1217A>G (p.Tyr406Cys) single nucleotide variant Inborn genetic diseases [RCV002932887]|not provided [RCV002932888] Chr19:48218957 [GRCh38]
Chr19:48722214 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.982G>A (p.Glu328Lys) single nucleotide variant not provided [RCV002791056] Chr19:48230491 [GRCh38]
Chr19:48733748 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.772+5T>C single nucleotide variant not provided [RCV002597355] Chr19:48230772 [GRCh38]
Chr19:48734029 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.318T>A (p.Pro106=) single nucleotide variant not provided [RCV002872616] Chr19:48234435 [GRCh38]
Chr19:48737692 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1468G>A (p.Glu490Lys) single nucleotide variant Inborn genetic diseases [RCV002919481]|not provided [RCV003679153] Chr19:48211856 [GRCh38]
Chr19:48715113 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.720G>A (p.Glu240=) single nucleotide variant not provided [RCV002643229] Chr19:48230829 [GRCh38]
Chr19:48734086 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1162-11G>A single nucleotide variant not provided [RCV002851917] Chr19:48219023 [GRCh38]
Chr19:48722280 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1027C>T (p.Leu343=) single nucleotide variant not provided [RCV002786296] Chr19:48230446 [GRCh38]
Chr19:48733703 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.668A>G (p.Gln223Arg) single nucleotide variant not provided [RCV002740734] Chr19:48230881 [GRCh38]
Chr19:48734138 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1374C>T (p.His458=) single nucleotide variant not provided [RCV002766635] Chr19:48211950 [GRCh38]
Chr19:48715207 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.663C>T (p.Asp221=) single nucleotide variant not provided [RCV003082654] Chr19:48230886 [GRCh38]
Chr19:48734143 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.963del (p.Tyr322fs) deletion not provided [RCV003040439] Chr19:48230510 [GRCh38]
Chr19:48733767 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.392G>A (p.Gly131Glu) single nucleotide variant not provided [RCV002643151] Chr19:48231810 [GRCh38]
Chr19:48735067 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.330A>G (p.Leu110=) single nucleotide variant not provided [RCV003043916] Chr19:48234423 [GRCh38]
Chr19:48737680 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.651C>T (p.His217=) single nucleotide variant not provided [RCV003047152] Chr19:48230898 [GRCh38]
Chr19:48734155 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.591C>T (p.Leu197=) single nucleotide variant not provided [RCV003092114] Chr19:48230958 [GRCh38]
Chr19:48734215 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.797T>G (p.Phe266Cys) single nucleotide variant not provided [RCV002938983] Chr19:48230676 [GRCh38]
Chr19:48733933 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.549G>T (p.Trp183Cys) single nucleotide variant not provided [RCV002647035] Chr19:48231000 [GRCh38]
Chr19:48734257 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.874G>C (p.Glu292Gln) single nucleotide variant Inborn genetic diseases [RCV002808434] Chr19:48230599 [GRCh38]
Chr19:48733856 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1036-12C>G single nucleotide variant not provided [RCV002598029] Chr19:48221867 [GRCh38]
Chr19:48725124 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.543C>T (p.Ser181=) single nucleotide variant not provided [RCV002577703] Chr19:48231006 [GRCh38]
Chr19:48734263 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.415C>T (p.Gln139Ter) single nucleotide variant not provided [RCV002601537] Chr19:48231787 [GRCh38]
Chr19:48735044 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1037C>T (p.Ala346Val) single nucleotide variant not provided [RCV002632004] Chr19:48221854 [GRCh38]
Chr19:48725111 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.851T>A (p.Val284Glu) single nucleotide variant not provided [RCV002811998] Chr19:48230622 [GRCh38]
Chr19:48733879 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.118C>T (p.Arg40Trp) single nucleotide variant CARD8-related condition [RCV003946390]|Inborn genetic diseases [RCV002964740] Chr19:48238474 [GRCh38]
Chr19:48741731 [GRCh37]
Chr19:19q13.33		 likely benign|uncertain significance
NM_001184900.3(CARD8):c.216C>G (p.Tyr72Ter) single nucleotide variant not provided [RCV002676120] Chr19:48234537 [GRCh38]
Chr19:48737794 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.83T>C (p.Ile28Thr) single nucleotide variant Inborn genetic diseases [RCV002657423] Chr19:48238509 [GRCh38]
Chr19:48741766 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.59+15G>A single nucleotide variant not provided [RCV002583449] Chr19:48240947 [GRCh38]
Chr19:48744204 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1057C>T (p.Arg353Cys) single nucleotide variant not provided [RCV002585252] Chr19:48221834 [GRCh38]
Chr19:48725091 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1376G>A (p.Arg459Gln) single nucleotide variant Inborn genetic diseases [RCV003250726]|not provided [RCV003071508] Chr19:48211948 [GRCh38]
Chr19:48715205 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.899G>T (p.Gly300Val) single nucleotide variant not provided [RCV002652970] Chr19:48230574 [GRCh38]
Chr19:48733831 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.17G>A (p.Cys6Tyr) single nucleotide variant not provided [RCV002608819] Chr19:48241004 [GRCh38]
Chr19:48744261 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.933C>T (p.Leu311=) single nucleotide variant not provided [RCV002589948] Chr19:48230540 [GRCh38]
Chr19:48733797 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1048G>A (p.Glu350Lys) single nucleotide variant not provided [RCV002942710] Chr19:48221843 [GRCh38]
Chr19:48725100 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1348+9A>G single nucleotide variant not provided [RCV002654278] Chr19:48215331 [GRCh38]
Chr19:48718588 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.711C>T (p.Val237=) single nucleotide variant not provided [RCV003071846] Chr19:48230838 [GRCh38]
Chr19:48734095 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1236A>T (p.Glu412Asp) single nucleotide variant not provided [RCV002587767] Chr19:48218938 [GRCh38]
Chr19:48722195 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.334G>C (p.Gly112Arg) single nucleotide variant not provided [RCV002612653] Chr19:48234419 [GRCh38]
Chr19:48737676 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.350+17C>T single nucleotide variant not provided [RCV002634572] Chr19:48234386 [GRCh38]
Chr19:48737643 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.767T>C (p.Leu256Pro) single nucleotide variant Inborn genetic diseases [RCV003197499] Chr19:48230782 [GRCh38]
Chr19:48734039 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.965A>G (p.Tyr322Cys) single nucleotide variant Inborn genetic diseases [RCV003346968] Chr19:48230508 [GRCh38]
Chr19:48733765 [GRCh37]
Chr19:19q13.33		 uncertain significance
NC_000019.10:g.48234544del deletion not provided [RCV003543172] Chr19:48234542 [GRCh38]
Chr19:48737799 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.391+9C>A single nucleotide variant not provided [RCV003571213] Chr19:48232444 [GRCh38]
Chr19:48735701 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.486G>C (p.Leu162=) single nucleotide variant not provided [RCV003570260] Chr19:48231716 [GRCh38]
Chr19:48734973 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1116del (p.Ser373fs) deletion not provided [RCV003686208] Chr19:48221775 [GRCh38]
Chr19:48725032 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1245A>C (p.Gln415His) single nucleotide variant not provided [RCV003686236] Chr19:48218929 [GRCh38]
Chr19:48722186 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1348+2dup duplication not provided [RCV003691146] Chr19:48215337..48215338 [GRCh38]
Chr19:48718594..48718595 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.266dup (p.Gln90fs) duplication CARD8-related condition [RCV003392922] Chr19:48234486..48234487 [GRCh38]
Chr19:48737743..48737744 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.559G>A (p.Ala187Thr) single nucleotide variant not provided [RCV003830518] Chr19:48230990 [GRCh38]
Chr19:48734247 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.849G>T (p.Arg283=) single nucleotide variant not provided [RCV003577707] Chr19:48230624 [GRCh38]
Chr19:48733881 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.456C>T (p.Ile152=) single nucleotide variant not provided [RCV003829118] Chr19:48231746 [GRCh38]
Chr19:48735003 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.248G>A (p.Cys83Tyr) single nucleotide variant not provided [RCV003694726] Chr19:48234505 [GRCh38]
Chr19:48737762 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.505G>A (p.Asp169Asn) single nucleotide variant not provided [RCV003577451] Chr19:48231697 [GRCh38]
Chr19:48734954 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.8A>G (p.Lys3Arg) single nucleotide variant not provided [RCV003830073] Chr19:48241013 [GRCh38]
Chr19:48744270 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1304-11C>T single nucleotide variant not provided [RCV003830282] Chr19:48215395 [GRCh38]
Chr19:48718652 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1009G>A (p.Val337Ile) single nucleotide variant not provided [RCV003695323] Chr19:48230464 [GRCh38]
Chr19:48733721 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.403T>C (p.Ser135Pro) single nucleotide variant not provided [RCV003830946] Chr19:48231799 [GRCh38]
Chr19:48735056 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1423C>T (p.Leu475Phe) single nucleotide variant not provided [RCV003829798] Chr19:48211901 [GRCh38]
Chr19:48715158 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.543-16C>T single nucleotide variant not provided [RCV003572046] Chr19:48231022 [GRCh38]
Chr19:48734279 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.630G>T (p.Ala210=) single nucleotide variant not provided [RCV003544857] Chr19:48230919 [GRCh38]
Chr19:48734176 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1349G>T (p.Gly450Val) single nucleotide variant not provided [RCV003686637] Chr19:48211975 [GRCh38]
Chr19:48715232 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.863A>C (p.Tyr288Ser) single nucleotide variant not provided [RCV003692206] Chr19:48230610 [GRCh38]
Chr19:48733867 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.339G>A (p.Gly113=) single nucleotide variant not provided [RCV003662900] Chr19:48234414 [GRCh38]
Chr19:48737671 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.476G>A (p.Arg159His) single nucleotide variant not provided [RCV003826172] Chr19:48231726 [GRCh38]
Chr19:48734983 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.59G>A (p.Arg20Gln) single nucleotide variant not provided [RCV003880824] Chr19:48240962 [GRCh38]
Chr19:48744219 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.748C>T (p.Leu250Phe) single nucleotide variant not provided [RCV003696955] Chr19:48230801 [GRCh38]
Chr19:48734058 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.998A>G (p.His333Arg) single nucleotide variant not provided [RCV003697304] Chr19:48230475 [GRCh38]
Chr19:48733732 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.850G>T (p.Val284Leu) single nucleotide variant not provided [RCV003579988] Chr19:48230623 [GRCh38]
Chr19:48733880 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.621G>A (p.Val207=) single nucleotide variant not provided [RCV003698470] Chr19:48230928 [GRCh38]
Chr19:48734185 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.363G>A (p.Glu121=) single nucleotide variant not provided [RCV003663911] Chr19:48232481 [GRCh38]
Chr19:48735738 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1493A>G (p.Lys498Arg) single nucleotide variant not provided [RCV003702932] Chr19:48211831 [GRCh38]
Chr19:48715088 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.34A>G (p.Ser12Gly) single nucleotide variant not provided [RCV003856867] Chr19:48240987 [GRCh38]
Chr19:48744244 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.426C>T (p.Ser142=) single nucleotide variant not provided [RCV003701930] Chr19:48231776 [GRCh38]
Chr19:48735033 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1002del (p.Leu334fs) deletion not provided [RCV003816801] Chr19:48230471 [GRCh38]
Chr19:48733728 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1002G>T (p.Leu334Phe) single nucleotide variant not provided [RCV003840139] Chr19:48230471 [GRCh38]
Chr19:48733728 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.869T>C (p.Val290Ala) single nucleotide variant not provided [RCV003670322] Chr19:48230604 [GRCh38]
Chr19:48733861 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.787G>A (p.Val263Ile) single nucleotide variant not provided [RCV003674168] Chr19:48230686 [GRCh38]
Chr19:48733943 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.256T>G (p.Ser86Ala) single nucleotide variant not provided [RCV003702607] Chr19:48234497 [GRCh38]
Chr19:48737754 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.762C>G (p.Ile254Met) single nucleotide variant not provided [RCV003664913] Chr19:48230787 [GRCh38]
Chr19:48734044 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.574_575del (p.Trp192fs) microsatellite not provided [RCV003702740] Chr19:48230974..48230975 [GRCh38]
Chr19:48734231..48734232 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1368G>C (p.Glu456Asp) single nucleotide variant not provided [RCV003672064] Chr19:48211956 [GRCh38]
Chr19:48715213 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1040T>C (p.Ile347Thr) single nucleotide variant not provided [RCV003699776] Chr19:48221851 [GRCh38]
Chr19:48725108 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.773-20C>T single nucleotide variant not provided [RCV003703080] Chr19:48230720 [GRCh38]
Chr19:48733977 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.383A>G (p.Gln128Arg) single nucleotide variant not provided [RCV003816513] Chr19:48232461 [GRCh38]
Chr19:48735718 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1474G>T (p.Glu492Ter) single nucleotide variant not provided [RCV003701019] Chr19:48211850 [GRCh38]
Chr19:48715107 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.706G>T (p.Asp236Tyr) single nucleotide variant not provided [RCV003580145] Chr19:48230843 [GRCh38]
Chr19:48734100 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.542+16G>A single nucleotide variant not provided [RCV003855335] Chr19:48231644 [GRCh38]
Chr19:48734901 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.273A>T (p.Glu91Asp) single nucleotide variant not provided [RCV003849794] Chr19:48234480 [GRCh38]
Chr19:48737737 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1036-10_1036-9delinsGT indel not provided [RCV003659259] Chr19:48221864..48221865 [GRCh38]
Chr19:48725121..48725122 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.351-15G>A single nucleotide variant not provided [RCV003832899] Chr19:48232508 [GRCh38]
Chr19:48735765 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.590T>C (p.Leu197Pro) single nucleotide variant not provided [RCV003659463] Chr19:48230959 [GRCh38]
Chr19:48734216 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1592A>G (p.Tyr531Cys) single nucleotide variant not provided [RCV003673087] Chr19:48211732 [GRCh38]
Chr19:48714989 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.412A>T (p.Asn138Tyr) single nucleotide variant not provided [RCV003839128] Chr19:48231790 [GRCh38]
Chr19:48735047 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1029A>G (p.Leu343=) single nucleotide variant not provided [RCV003552126] Chr19:48230444 [GRCh38]
Chr19:48733701 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1476A>G (p.Glu492=) single nucleotide variant not provided [RCV003858424] Chr19:48211848 [GRCh38]
Chr19:48715105 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.772+10G>A single nucleotide variant not provided [RCV003563175] Chr19:48230767 [GRCh38]
Chr19:48734024 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1288A>G (p.Thr430Ala) single nucleotide variant not provided [RCV003552350] Chr19:48218886 [GRCh38]
Chr19:48722143 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.290C>T (p.Ala97Val) single nucleotide variant not provided [RCV003568117] Chr19:48234463 [GRCh38]
Chr19:48737720 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.909G>A (p.Leu303=) single nucleotide variant not provided [RCV003858314] Chr19:48230564 [GRCh38]
Chr19:48733821 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.840T>C (p.His280=) single nucleotide variant not provided [RCV003705670] Chr19:48230633 [GRCh38]
Chr19:48733890 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.271G>A (p.Glu91Lys) single nucleotide variant not provided [RCV003843644] Chr19:48234482 [GRCh38]
Chr19:48737739 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1438G>C (p.Val480Leu) single nucleotide variant not provided [RCV003550774] Chr19:48211886 [GRCh38]
Chr19:48715143 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.738C>T (p.Ala246=) single nucleotide variant not provided [RCV003734155] Chr19:48230811 [GRCh38]
Chr19:48734068 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.466del (p.Tyr156fs) deletion not provided [RCV003822167] Chr19:48231736 [GRCh38]
Chr19:48734993 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.468T>C (p.Tyr156=) single nucleotide variant not provided [RCV003683797] Chr19:48231734 [GRCh38]
Chr19:48734991 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.360A>G (p.Glu120=) single nucleotide variant not provided [RCV003822353] Chr19:48232484 [GRCh38]
Chr19:48735741 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.534C>A (p.Asn178Lys) single nucleotide variant not provided [RCV003678563] Chr19:48231668 [GRCh38]
Chr19:48734925 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1059C>T (p.Arg353=) single nucleotide variant not provided [RCV003686141] Chr19:48221832 [GRCh38]
Chr19:48725089 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1346C>T (p.Ser449Leu) single nucleotide variant not provided [RCV003847707] Chr19:48215342 [GRCh38]
Chr19:48718599 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.456C>G (p.Ile152Met) single nucleotide variant not provided [RCV003684831] Chr19:48231746 [GRCh38]
Chr19:48735003 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1360G>A (p.Val454Met) single nucleotide variant not provided [RCV003854062] Chr19:48211964 [GRCh38]
Chr19:48715221 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.713C>G (p.Thr238Ser) single nucleotide variant not provided [RCV003841390] Chr19:48230836 [GRCh38]
Chr19:48734093 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1556G>T (p.Arg519Ile) single nucleotide variant not provided [RCV003872340] Chr19:48211768 [GRCh38]
Chr19:48715025 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.974C>T (p.Pro325Leu) single nucleotide variant not provided [RCV003820640] Chr19:48230499 [GRCh38]
Chr19:48733756 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.351-10C>T single nucleotide variant not provided [RCV003737129] Chr19:48232503 [GRCh38]
Chr19:48735760 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1073G>A (p.Arg358His) single nucleotide variant not provided [RCV003870935] Chr19:48221818 [GRCh38]
Chr19:48725075 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1047T>A (p.Asp349Glu) single nucleotide variant not provided [RCV003859436] Chr19:48221844 [GRCh38]
Chr19:48725101 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.704T>C (p.Phe235Ser) single nucleotide variant not provided [RCV003719099] Chr19:48230845 [GRCh38]
Chr19:48734102 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.831C>T (p.Val277=) single nucleotide variant not provided [RCV003706267] Chr19:48230642 [GRCh38]
Chr19:48733899 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1036-5C>T single nucleotide variant not provided [RCV003721553] Chr19:48221860 [GRCh38]
Chr19:48725117 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.473A>G (p.Asn158Ser) single nucleotide variant not provided [RCV003684182] Chr19:48231729 [GRCh38]
Chr19:48734986 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.537A>G (p.Arg179=) single nucleotide variant not provided [RCV003721684] Chr19:48231665 [GRCh38]
Chr19:48734922 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1161G>T (p.Lys387Asn) single nucleotide variant not provided [RCV003847314] Chr19:48221730 [GRCh38]
Chr19:48724987 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.447T>A (p.Cys149Ter) single nucleotide variant not provided [RCV003738575] Chr19:48231755 [GRCh38]
Chr19:48735012 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.340dup (p.Asp114fs) duplication not provided [RCV003722042] Chr19:48234412..48234413 [GRCh38]
Chr19:48737669..48737670 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.287_288del (p.Glu96fs) microsatellite not provided [RCV003554197] Chr19:48234465..48234466 [GRCh38]
Chr19:48737722..48737723 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.334G>T (p.Gly112Trp) single nucleotide variant not provided [RCV003709957] Chr19:48234419 [GRCh38]
Chr19:48737676 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1304-14del deletion not provided [RCV003680104] Chr19:48215398 [GRCh38]
Chr19:48718655 [GRCh37]
Chr19:19q13.33		 benign
NM_001184900.3(CARD8):c.915C>G (p.Ile305Met) single nucleotide variant not provided [RCV003733757] Chr19:48230558 [GRCh38]
Chr19:48733815 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.772+17G>A single nucleotide variant not provided [RCV003864306] Chr19:48230760 [GRCh38]
Chr19:48734017 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1502C>A (p.Ala501Asp) single nucleotide variant not provided [RCV003821927] Chr19:48211822 [GRCh38]
Chr19:48715079 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.878G>T (p.Ser293Ile) single nucleotide variant not provided [RCV003567978] Chr19:48230595 [GRCh38]
Chr19:48733852 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.879C>T (p.Ser293=) single nucleotide variant not provided [RCV003864447] Chr19:48230594 [GRCh38]
Chr19:48733851 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.900C>T (p.Gly300=) single nucleotide variant not provided [RCV003562560] Chr19:48230573 [GRCh38]
Chr19:48733830 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1262A>G (p.Lys421Arg) single nucleotide variant not provided [RCV003708209] Chr19:48218912 [GRCh38]
Chr19:48722169 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.223C>T (p.Leu75=) single nucleotide variant not provided [RCV003550536] Chr19:48234530 [GRCh38]
Chr19:48737787 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.230G>C (p.Cys77Ser) single nucleotide variant not provided [RCV003845200] Chr19:48234523 [GRCh38]
Chr19:48737780 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.1546G>A (p.Val516Met) single nucleotide variant not provided [RCV003860064] Chr19:48211778 [GRCh38]
Chr19:48715035 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.479A>G (p.Gln160Arg) single nucleotide variant not provided [RCV003678770] Chr19:48231723 [GRCh38]
Chr19:48734980 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.54G>A (p.Pro18=) single nucleotide variant not provided [RCV003823079] Chr19:48240967 [GRCh38]
Chr19:48744224 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.282G>C (p.Glu94Asp) single nucleotide variant not provided [RCV003668520] Chr19:48234471 [GRCh38]
Chr19:48737728 [GRCh37]
Chr19:19q13.33		 uncertain significance
GRCh37/hg19 19q13.32-13.42(chr19:47939842-54626871) copy number gain not provided [RCV001249294] Chr19:47939842..54626871 [GRCh37]
Chr19:19q13.32-13.42		 not provided
NM_001184900.3(CARD8):c.694G>A (p.Gly232Ser) single nucleotide variant not provided [RCV001926453] Chr19:48230855 [GRCh38]
Chr19:48734112 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.957A>G (p.Thr319=) single nucleotide variant not provided [RCV002111290] Chr19:48230516 [GRCh38]
Chr19:48733773 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.210-17C>G single nucleotide variant not provided [RCV002087246] Chr19:48234560 [GRCh38]
Chr19:48737817 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.351-20A>G single nucleotide variant not provided [RCV002146129] Chr19:48232513 [GRCh38]
Chr19:48735770 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.1162-4C>T single nucleotide variant not provided [RCV003012163] Chr19:48219016 [GRCh38]
Chr19:48722273 [GRCh37]
Chr19:19q13.33		 likely benign
NM_001184900.3(CARD8):c.485T>C (p.Leu162Pro) single nucleotide variant not provided [RCV002721676] Chr19:48231717 [GRCh38]
Chr19:48734974 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.145C>T (p.Arg49Trp) single nucleotide variant Inborn genetic diseases [RCV003256810] Chr19:48238447 [GRCh38]
Chr19:48741704 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.150A>T (p.Glu50Asp) single nucleotide variant Inborn genetic diseases [RCV003210108] Chr19:48238442 [GRCh38]
Chr19:48741699 [GRCh37]
Chr19:19q13.33		 uncertain significance
NM_001184900.3(CARD8):c.576G>C (p.Trp192Cys) single nucleotide variant Inborn genetic diseases [RCV003360173] Chr19:48230973 [GRCh38]
Chr19:48734230 [GRCh37]
Chr19:19q13.33		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:13351
Count of miRNA genes:1316
Interacting mature miRNAs:1734
Transcripts:ENST00000357778, ENST00000359009, ENST00000377461, ENST00000391898, ENST00000447740, ENST00000517510, ENST00000517778, ENST00000518450, ENST00000518596, ENST00000518622, ENST00000518979, ENST00000519302, ENST00000519332, ENST00000519646, ENST00000519940, ENST00000520007, ENST00000520015, ENST00000520153, ENST00000520753, ENST00000521092, ENST00000521415, ENST00000521437, ENST00000521613, ENST00000522051, ENST00000522068, ENST00000522431, ENST00000522773, ENST00000522889, ENST00000523579, ENST00000523668, ENST00000523750, ENST00000600800
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
D19S1113  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371948,741,614 - 48,741,754UniSTSGRCh37
Build 361953,433,426 - 53,433,566RGDNCBI36
Celera1945,606,850 - 45,606,990RGD
Cytogenetic Map19q13.33UniSTS
HuRef1945,123,581 - 45,123,721UniSTS
Stanford-G3 RH Map192450.0UniSTS
NCBI RH Map19537.6UniSTS
GeneMap99-G3 RH Map192461.0UniSTS
D19S1010  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371948,741,614 - 48,741,738UniSTSGRCh37
Build 361953,433,426 - 53,433,550RGDNCBI36
Celera1945,606,850 - 45,606,974RGD
Cytogenetic Map19q13.33UniSTS
HuRef1945,123,581 - 45,123,705UniSTS
RH16607  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371948,706,520 - 48,706,708UniSTSGRCh37
Build 361953,398,332 - 53,398,520RGDNCBI36
Celera1945,571,746 - 45,571,934RGD
Cytogenetic Map19q13.33UniSTS
HuRef1945,088,464 - 45,088,652UniSTS
GeneMap99-GB4 RH Map19266.52UniSTS
WI-14251  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371948,714,071 - 48,714,197UniSTSGRCh37
Build 361953,405,883 - 53,406,009RGDNCBI36
Celera1945,579,295 - 45,579,421RGD
Cytogenetic Map19q13.33UniSTS
HuRef1945,096,031 - 45,096,157UniSTS
GeneMap99-GB4 RH Map19266.73UniSTS
Whitehead-RH Map19343.4UniSTS
SHGC-33567  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371948,706,432 - 48,706,557UniSTSGRCh37
Build 361953,398,244 - 53,398,369RGDNCBI36
Celera1945,571,658 - 45,571,783RGD
Cytogenetic Map19q13.33UniSTS
HuRef1945,088,376 - 45,088,501UniSTS
GeneMap99-GB4 RH Map19266.31UniSTS
Whitehead-RH Map19341.9UniSTS
GeneMap99-G3 RH Map192459.0UniSTS
GDB:434012  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map2q31.2-q33.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map5q21UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map1p21.3-p13.1UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map1q24-q25.3UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1pter-q31.3UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map16p13UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map10p11.1UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map2q11.2-q12UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic MapXq21.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map4p16UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map14q31UniSTS
GDB:312794  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map14q24.3UniSTS
RH36905  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map18p11.3-p11.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map3q27-q28UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map3q26.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map3q12.2-q12.3UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q12-q13.1UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map9q31.1UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map10q21UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map10q24.1UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map10q25-q26UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map16q22.1UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 515 757 636 48 1560 40 1155 263 539 83 502 1116 9 980 547 1
Low 1923 2234 1090 576 391 425 3200 1934 3195 336 957 495 165 1 224 2241 5 2
Below cutoff 1 1 1 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_029574 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001184900 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001184901 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001184902 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001184903 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001184904 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351782 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351783 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351784 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351786 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351787 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351788 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351789 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351790 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351791 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351792 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001365950 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001426741 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_014959 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_033678 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_033679 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_033680 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_147707 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006723091 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006723092 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006723093 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006723094 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006723096 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006723097 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006723098 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006723102 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006723104 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006723106 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006723107 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006723109 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006723110 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526641 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526643 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526644 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526646 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526647 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526648 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526650 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026482 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026483 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026484 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026485 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026487 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026488 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026492 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026498 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026499 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024451421 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024451422 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024451423 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024451424 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024451425 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438434 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438435 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438436 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438437 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438438 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438439 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438440 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438441 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438442 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438443 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438444 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438445 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438446 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438447 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438448 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438449 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438450 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438451 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438452 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438453 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438454 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438455 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438456 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438457 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438458 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438459 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438460 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438461 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438462 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438463 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438464 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438465 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320231 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320232 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320233 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320234 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320235 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320236 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320237 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320238 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320239 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320240 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320241 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320242 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320243 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320244 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320245 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320246 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320247 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320248 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320249 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320250 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320251 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320252 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320253 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320254 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320255 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320256 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320257 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320258 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320260 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320262 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320263 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320264 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320265 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320266 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320268 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320270 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001753636 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001753637 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008485122 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008485123 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008485124 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008485125 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_430193 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB023172 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC008392 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC011466 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF143869 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF322184 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF331519 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF405558 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF511652 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI040349 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK094933 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297045 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297069 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302327 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK311077 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK311079 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AX089767 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY026322 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC034564 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC041697 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC045539 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC046136 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC056891 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX641091 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX648568 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA389350 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA448628 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB119078 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471177 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR983845 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA675182 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC347384 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC382648 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC404273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU118120 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU118121 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU118122 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000377461
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,209,644 - 48,232,114 (-)Ensembl
RefSeq Acc Id: ENST00000391898   ⟹   ENSP00000375767
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,208,104 - 48,241,063 (-)Ensembl
RefSeq Acc Id: ENST00000447740   ⟹   ENSP00000391248
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,208,104 - 48,249,847 (-)Ensembl
RefSeq Acc Id: ENST00000517510   ⟹   ENSP00000428662
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,203,632 - 48,255,898 (-)Ensembl
RefSeq Acc Id: ENST00000517778
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,233,846 - 48,249,614 (-)Ensembl
RefSeq Acc Id: ENST00000518450   ⟹   ENSP00000428975
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,203,146 - 48,218,953 (-)Ensembl
RefSeq Acc Id: ENST00000518596
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,233,821 - 48,249,828 (-)Ensembl
RefSeq Acc Id: ENST00000518622   ⟹   ENSP00000430057
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,208,086 - 48,249,668 (-)Ensembl
RefSeq Acc Id: ENST00000518979   ⟹   ENSP00000430495
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,209,644 - 48,249,668 (-)Ensembl
RefSeq Acc Id: ENST00000519302   ⟹   ENSP00000429741
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,211,897 - 48,249,816 (-)Ensembl
RefSeq Acc Id: ENST00000519332   ⟹   ENSP00000430108
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,238,334 - 48,255,893 (-)Ensembl
RefSeq Acc Id: ENST00000519646   ⟹   ENSP00000430836
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,211,152 - 48,249,826 (-)Ensembl
RefSeq Acc Id: ENST00000519940   ⟹   ENSP00000428883
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,209,668 - 48,255,873 (-)Ensembl
RefSeq Acc Id: ENST00000520007   ⟹   ENSP00000427727
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,238,336 - 48,255,898 (-)Ensembl
RefSeq Acc Id: ENST00000520015   ⟹   ENSP00000430747
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,211,377 - 48,249,833 (-)Ensembl
RefSeq Acc Id: ENST00000520153   ⟹   ENSP00000428736
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,210,787 - 48,249,826 (-)Ensembl
RefSeq Acc Id: ENST00000520753   ⟹   ENSP00000429839
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,210,487 - 48,255,886 (-)Ensembl
RefSeq Acc Id: ENST00000521092
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,234,278 - 48,249,826 (-)Ensembl
RefSeq Acc Id: ENST00000521415   ⟹   ENSP00000428862
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,211,617 - 48,241,063 (-)Ensembl
RefSeq Acc Id: ENST00000521437   ⟹   ENSP00000430178
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,238,475 - 48,255,897 (-)Ensembl
RefSeq Acc Id: ENST00000521613   ⟹   ENSP00000427858
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,211,566 - 48,255,946 (-)Ensembl
RefSeq Acc Id: ENST00000522051
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,210,790 - 48,249,833 (-)Ensembl
RefSeq Acc Id: ENST00000522068
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,231,729 - 48,255,911 (-)Ensembl
RefSeq Acc Id: ENST00000522431   ⟹   ENSP00000427922
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,238,262 - 48,249,771 (-)Ensembl
RefSeq Acc Id: ENST00000522773   ⟹   ENSP00000429362
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,210,787 - 48,249,810 (-)Ensembl
RefSeq Acc Id: ENST00000522889   ⟹   ENSP00000430567
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,234,472 - 48,255,871 (-)Ensembl
RefSeq Acc Id: ENST00000523579   ⟹   ENSP00000430460
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,211,827 - 48,230,498 (-)Ensembl
RefSeq Acc Id: ENST00000523668
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,215,138 - 48,230,647 (-)Ensembl
RefSeq Acc Id: ENST00000523750
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,233,410 - 48,234,464 (-)Ensembl
RefSeq Acc Id: ENST00000600800
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,180,770 - 48,203,952 (-)Ensembl
RefSeq Acc Id: ENST00000651546   ⟹   ENSP00000499211
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1948,208,086 - 48,255,912 (-)Ensembl
RefSeq Acc Id: NM_001184900   ⟹   NP_001171829
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,912 (-)NCBI
GRCh371948,711,343 - 48,759,203 (-)ENTREZGENE
HuRef1945,093,304 - 45,141,176 (-)ENTREZGENE
CHM1_11948,713,493 - 48,746,462 (-)NCBI
T2T-CHM13v2.01951,202,167 - 51,250,019 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001184901   ⟹   NP_001171830
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,249,847 (-)NCBI
GRCh371948,711,343 - 48,759,203 (-)ENTREZGENE
HuRef1945,093,304 - 45,141,176 (-)ENTREZGENE
CHM1_11948,713,493 - 48,755,246 (-)NCBI
T2T-CHM13v2.01951,202,167 - 51,243,939 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001184902   ⟹   NP_001171831
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,912 (-)NCBI
GRCh371948,711,343 - 48,759,203 (-)ENTREZGENE
HuRef1945,093,304 - 45,141,176 (-)ENTREZGENE
CHM1_11948,713,493 - 48,761,345 (-)NCBI
T2T-CHM13v2.01951,202,167 - 51,250,019 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001184903   ⟹   NP_001171832
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,249,847 (-)NCBI
GRCh371948,711,343 - 48,759,203 (-)ENTREZGENE
HuRef1945,093,304 - 45,141,176 (-)ENTREZGENE
CHM1_11948,713,493 - 48,755,246 (-)NCBI
T2T-CHM13v2.01951,202,167 - 51,243,939 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001184904   ⟹   NP_001171833
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,238,261 - 48,255,912 (-)NCBI
GRCh371948,711,343 - 48,759,203 (-)ENTREZGENE
HuRef1945,093,304 - 45,141,176 (-)ENTREZGENE
CHM1_11948,743,660 - 48,761,345 (-)NCBI
T2T-CHM13v2.01951,232,356 - 51,250,019 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001351782   ⟹   NP_001338711
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,912 (-)NCBI
T2T-CHM13v2.01951,202,167 - 51,250,019 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001351783   ⟹   NP_001338712
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,912 (-)NCBI
T2T-CHM13v2.01951,202,167 - 51,250,019 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001351784   ⟹   NP_001338713
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,912 (-)NCBI
T2T-CHM13v2.01951,202,167 - 51,250,019 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001351786   ⟹   NP_001338715
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,912 (-)NCBI
T2T-CHM13v2.01951,202,167 - 51,250,019 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001351787   ⟹   NP_001338716
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,203,148 - 48,255,912 (-)NCBI
T2T-CHM13v2.01951,197,212 - 51,250,019 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001351788   ⟹   NP_001338717
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,912 (-)NCBI
T2T-CHM13v2.01951,202,167 - 51,250,019 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001351789   ⟹   NP_001338718
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,912 (-)NCBI
T2T-CHM13v2.01951,202,167 - 51,250,019 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001351790   ⟹   NP_001338719
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,912 (-)NCBI
T2T-CHM13v2.01951,202,167 - 51,250,019 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001351791   ⟹   NP_001338720
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,912 (-)NCBI
T2T-CHM13v2.01951,202,167 - 51,250,019 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001351792   ⟹   NP_001338721
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,912 (-)NCBI
T2T-CHM13v2.01951,202,167 - 51,250,019 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001365950   ⟹   NP_001352879
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,249,828 (-)NCBI
T2T-CHM13v2.01951,202,167 - 51,243,920 (-)NCBI
Sequence:
RefSeq Acc Id: NM_014959   ⟹   NP_055774
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,912 (-)NCBI
GRCh371948,711,343 - 48,759,203 (-)ENTREZGENE
Build 361953,403,325 - 53,444,737 (-)NCBI Archive
HuRef1945,093,304 - 45,141,176 (-)ENTREZGENE
CHM1_11948,713,493 - 48,755,246 (-)NCBI
T2T-CHM13v2.01951,202,167 - 51,250,019 (-)NCBI
Sequence:
RefSeq Acc Id: NR_033678
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,249,633 (-)NCBI
GRCh371948,711,343 - 48,759,203 (-)ENTREZGENE
HuRef1945,093,304 - 45,141,176 (-)ENTREZGENE
CHM1_11948,713,493 - 48,755,032 (-)NCBI
T2T-CHM13v2.01951,202,167 - 51,243,725 (-)NCBI
Sequence:
RefSeq Acc Id: NR_033679
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,241,063 (-)NCBI
GRCh371948,711,343 - 48,759,203 (-)ENTREZGENE
HuRef1945,093,304 - 45,141,176 (-)ENTREZGENE
CHM1_11948,713,493 - 48,746,462 (-)NCBI
T2T-CHM13v2.01951,202,167 - 51,235,157 (-)NCBI
Sequence:
RefSeq Acc Id: NR_033680
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,249,633 (-)NCBI
GRCh371948,711,343 - 48,759,203 (-)ENTREZGENE
HuRef1945,093,304 - 45,141,176 (-)ENTREZGENE
CHM1_11948,713,493 - 48,755,032 (-)NCBI
T2T-CHM13v2.01951,202,167 - 51,243,725 (-)NCBI
Sequence:
RefSeq Acc Id: NR_147707
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,203,148 - 48,255,946 (-)NCBI
T2T-CHM13v2.01951,197,212 - 51,250,053 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006723092   ⟹   XP_006723155
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006723093   ⟹   XP_006723156
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006723096   ⟹   XP_006723159
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006723097   ⟹   XP_006723160
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006723110   ⟹   XP_006723173
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,223,726 - 48,255,946 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011526641   ⟹   XP_011524943
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011526643   ⟹   XP_011524945
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011526650   ⟹   XP_011524952
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,206,503 - 48,255,946 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017026482   ⟹   XP_016881971
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017026483   ⟹   XP_016881972
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017026484   ⟹   XP_016881973
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017026485   ⟹   XP_016881974
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,203,148 - 48,255,946 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017026487   ⟹   XP_016881976
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,234,511 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047438434   ⟹   XP_047294390
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438435   ⟹   XP_047294391
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438436   ⟹   XP_047294392
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438437   ⟹   XP_047294393
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438438   ⟹   XP_047294394
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438439   ⟹   XP_047294395
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438440   ⟹   XP_047294396
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438441   ⟹   XP_047294397
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438442   ⟹   XP_047294398
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438443   ⟹   XP_047294399
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438444   ⟹   XP_047294400
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438445   ⟹   XP_047294401
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438446   ⟹   XP_047294402
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438447   ⟹   XP_047294403
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438448   ⟹   XP_047294404
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438449   ⟹   XP_047294405
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438450   ⟹   XP_047294406
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438451   ⟹   XP_047294407
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438452   ⟹   XP_047294408
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438453   ⟹   XP_047294409
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,205,186 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438454   ⟹   XP_047294410
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,205,186 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438455   ⟹   XP_047294411
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,203,148 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438456   ⟹   XP_047294412
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,238,349 (-)NCBI
RefSeq Acc Id: XM_047438457   ⟹   XP_047294413
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,238,352 (-)NCBI
RefSeq Acc Id: XM_047438458   ⟹   XP_047294414
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,238,533 (-)NCBI
RefSeq Acc Id: XM_047438459   ⟹   XP_047294415
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438460   ⟹   XP_047294416
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,208,086 - 48,234,492 (-)NCBI
RefSeq Acc Id: XM_047438461   ⟹   XP_047294417
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,205,186 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438462   ⟹   XP_047294418
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,218,871 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438463   ⟹   XP_047294419
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,206,506 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438464   ⟹   XP_047294420
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,223,726 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_047438465   ⟹   XP_047294421
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,218,871 - 48,255,946 (-)NCBI
RefSeq Acc Id: XM_054320231   ⟹   XP_054176206
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320232   ⟹   XP_054176207
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320233   ⟹   XP_054176208
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320234   ⟹   XP_054176209
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320235   ⟹   XP_054176210
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320236   ⟹   XP_054176211
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320237   ⟹   XP_054176212
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320238   ⟹   XP_054176213
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320239   ⟹   XP_054176214
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320240   ⟹   XP_054176215
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320241   ⟹   XP_054176216
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320242   ⟹   XP_054176217
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320243   ⟹   XP_054176218
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320244   ⟹   XP_054176219
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320245   ⟹   XP_054176220
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320246   ⟹   XP_054176221
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320247   ⟹   XP_054176222
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320248   ⟹   XP_054176223
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320249   ⟹   XP_054176224
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320250   ⟹   XP_054176225
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320251   ⟹   XP_054176226
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320252   ⟹   XP_054176227
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320253   ⟹   XP_054176228
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320254   ⟹   XP_054176229
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320255   ⟹   XP_054176230
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320256   ⟹   XP_054176231
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320257   ⟹   XP_054176232
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320258   ⟹   XP_054176233
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320259   ⟹   XP_054176234
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,199,250 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320260   ⟹   XP_054176235
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,199,250 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320261   ⟹   XP_054176236
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,197,212 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320262   ⟹   XP_054176237
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,197,212 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320263   ⟹   XP_054176238
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,232,443 (-)NCBI
RefSeq Acc Id: XM_054320264   ⟹   XP_054176239
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,232,443 (-)NCBI
RefSeq Acc Id: XM_054320265   ⟹   XP_054176240
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,232,447 (-)NCBI
RefSeq Acc Id: XM_054320266   ⟹   XP_054176241
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,199,250 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320267   ⟹   XP_054176242
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,202,167 - 51,232,444 (-)NCBI
RefSeq Acc Id: XM_054320268   ⟹   XP_054176243
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,200,567 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320269   ⟹   XP_054176244
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,212,945 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320270   ⟹   XP_054176245
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,200,570 - 51,250,053 (-)NCBI
RefSeq Acc Id: XM_054320271   ⟹   XP_054176246
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,212,945 - 51,250,053 (-)NCBI
RefSeq Acc Id: XR_001753636
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,179,825 - 48,255,946 (-)NCBI
Sequence:
RefSeq Acc Id: XR_008485122
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,198,222 - 51,250,053 (-)NCBI
RefSeq Acc Id: XR_008485123
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,215,860 - 51,250,053 (-)NCBI
RefSeq Acc Id: XR_008485124
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,215,860 - 51,250,053 (-)NCBI
RefSeq Acc Id: XR_008485125
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01951,215,860 - 51,250,053 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001171829 (Get FASTA)   NCBI Sequence Viewer  
  NP_001171830 (Get FASTA)   NCBI Sequence Viewer  
  NP_001171831 (Get FASTA)   NCBI Sequence Viewer  
  NP_001171832 (Get FASTA)   NCBI Sequence Viewer  
  NP_001171833 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338711 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338712 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338713 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338715 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338716 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338717 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338718 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338719 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338720 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338721 (Get FASTA)   NCBI Sequence Viewer  
  NP_001352879 (Get FASTA)   NCBI Sequence Viewer  
  NP_001413670 (Get FASTA)   NCBI Sequence Viewer  
  NP_055774 (Get FASTA)   NCBI Sequence Viewer  
  XP_006723155 (Get FASTA)   NCBI Sequence Viewer  
  XP_006723156 (Get FASTA)   NCBI Sequence Viewer  
  XP_006723159 (Get FASTA)   NCBI Sequence Viewer  
  XP_006723160 (Get FASTA)   NCBI Sequence Viewer  
  XP_006723173 (Get FASTA)   NCBI Sequence Viewer  
  XP_011524943 (Get FASTA)   NCBI Sequence Viewer  
  XP_011524945 (Get FASTA)   NCBI Sequence Viewer  
  XP_011524952 (Get FASTA)   NCBI Sequence Viewer  
  XP_016881971 (Get FASTA)   NCBI Sequence Viewer  
  XP_016881972 (Get FASTA)   NCBI Sequence Viewer  
  XP_016881973 (Get FASTA)   NCBI Sequence Viewer  
  XP_016881974 (Get FASTA)   NCBI Sequence Viewer  
  XP_016881976 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294390 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294391 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294392 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294393 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294394 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294395 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294396 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294397 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294398 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294399 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294400 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294401 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294402 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294403 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294404 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294405 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294406 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294407 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294408 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294409 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294410 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294411 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294412 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294413 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294414 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294415 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294416 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294417 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294418 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294419 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294420 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294421 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176206 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176207 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176208 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176209 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176210 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176211 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176212 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176213 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176214 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176215 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176216 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176217 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176218 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176219 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176220 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176221 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176222 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176223 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176224 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176225 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176226 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176227 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176228 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176229 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176230 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176231 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176232 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176233 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176234 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176235 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176236 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176237 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176238 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176239 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176240 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176241 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176242 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176243 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176244 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176245 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176246 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAG50014 (Get FASTA)   NCBI Sequence Viewer  
  AAH45539 (Get FASTA)   NCBI Sequence Viewer  
  AAH56891 (Get FASTA)   NCBI Sequence Viewer  
  AAK01126 (Get FASTA)   NCBI Sequence Viewer  
  AAK08982 (Get FASTA)   NCBI Sequence Viewer  
  AAL02427 (Get FASTA)   NCBI Sequence Viewer  
  AAM46959 (Get FASTA)   NCBI Sequence Viewer  
  ABW96891 (Get FASTA)   NCBI Sequence Viewer  
  ABW96892 (Get FASTA)   NCBI Sequence Viewer  
  ABW96893 (Get FASTA)   NCBI Sequence Viewer  
  BAA76799 (Get FASTA)   NCBI Sequence Viewer  
  BAH12482 (Get FASTA)   NCBI Sequence Viewer  
  BAH12488 (Get FASTA)   NCBI Sequence Viewer  
  BAH13675 (Get FASTA)   NCBI Sequence Viewer  
  CAC34902 (Get FASTA)   NCBI Sequence Viewer  
  CAE46043 (Get FASTA)   NCBI Sequence Viewer  
  EAW52319 (Get FASTA)   NCBI Sequence Viewer  
  EAW52320 (Get FASTA)   NCBI Sequence Viewer  
  EAW52321 (Get FASTA)   NCBI Sequence Viewer  
  EAW52322 (Get FASTA)   NCBI Sequence Viewer  
  EAW52323 (Get FASTA)   NCBI Sequence Viewer  
  EAW52324 (Get FASTA)   NCBI Sequence Viewer  
  EAW52325 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000375767
  ENSP00000375767.3
  ENSP00000391248
  ENSP00000391248.2
  ENSP00000427727.1
  ENSP00000427858
  ENSP00000427858.1
  ENSP00000427922.1
  ENSP00000428662.1
  ENSP00000428736
  ENSP00000428736.1
  ENSP00000428862.1
  ENSP00000428883
  ENSP00000428883.1
  ENSP00000428975.1
  ENSP00000429362.1
  ENSP00000429741.1
  ENSP00000429839
  ENSP00000429839.1
  ENSP00000430057.1
  ENSP00000430108
  ENSP00000430108.1
  ENSP00000430178.1
  ENSP00000430460.1
  ENSP00000430495.1
  ENSP00000430567.1
  ENSP00000430747
  ENSP00000430747.1
  ENSP00000430836.1
  ENSP00000499211
  ENSP00000499211.1
GenBank Protein Q9Y2G2 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_001171831   ⟸   NM_001184902
- Peptide Label: isoform c
- UniProtKB: Q9Y2G2 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001171830   ⟸   NM_001184901
- Peptide Label: isoform b
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001171832   ⟸   NM_001184903
- Peptide Label: isoform c
- UniProtKB: Q9Y2G2 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_055774   ⟸   NM_014959
- Peptide Label: isoform b
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001171829   ⟸   NM_001184900
- Peptide Label: isoform a
- UniProtKB: Q6PGP8 (UniProtKB/Swiss-Prot),   G3XAM9 (UniProtKB/Swiss-Prot),   E9PEM7 (UniProtKB/Swiss-Prot),   E5RFV9 (UniProtKB/Swiss-Prot),   B7Z4A2 (UniProtKB/Swiss-Prot),   B7Z496 (UniProtKB/Swiss-Prot),   B5KVR8 (UniProtKB/Swiss-Prot),   B5KVR6 (UniProtKB/Swiss-Prot),   Q96P82 (UniProtKB/Swiss-Prot),   Q9Y2G2 (UniProtKB/Swiss-Prot),   I6L9C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001171833   ⟸   NM_001184904
- Peptide Label: isoform d
- UniProtKB: E5RFV9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006723160   ⟸   XM_006723097
- Peptide Label: isoform X3
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006723156   ⟸   XM_006723093
- Peptide Label: isoform X1
- UniProtKB: Q6PGP8 (UniProtKB/Swiss-Prot),   G3XAM9 (UniProtKB/Swiss-Prot),   E9PEM7 (UniProtKB/Swiss-Prot),   E5RFV9 (UniProtKB/Swiss-Prot),   B7Z4A2 (UniProtKB/Swiss-Prot),   B7Z496 (UniProtKB/Swiss-Prot),   B5KVR8 (UniProtKB/Swiss-Prot),   B5KVR6 (UniProtKB/Swiss-Prot),   Q96P82 (UniProtKB/Swiss-Prot),   Q9Y2G2 (UniProtKB/Swiss-Prot),   I6L9C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006723155   ⟸   XM_006723092
- Peptide Label: isoform X1
- UniProtKB: Q6PGP8 (UniProtKB/Swiss-Prot),   G3XAM9 (UniProtKB/Swiss-Prot),   E9PEM7 (UniProtKB/Swiss-Prot),   E5RFV9 (UniProtKB/Swiss-Prot),   B7Z4A2 (UniProtKB/Swiss-Prot),   B7Z496 (UniProtKB/Swiss-Prot),   B5KVR8 (UniProtKB/Swiss-Prot),   B5KVR6 (UniProtKB/Swiss-Prot),   Q96P82 (UniProtKB/Swiss-Prot),   Q9Y2G2 (UniProtKB/Swiss-Prot),   I6L9C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006723159   ⟸   XM_006723096
- Peptide Label: isoform X3
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006723173   ⟸   XM_006723110
- Peptide Label: isoform X17
- Sequence:
RefSeq Acc Id: XP_011524952   ⟸   XM_011526650
- Peptide Label: isoform X14
- UniProtKB: Q9Y2G2 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011524945   ⟸   XM_011526643
- Peptide Label: isoform X1
- UniProtKB: Q6PGP8 (UniProtKB/Swiss-Prot),   G3XAM9 (UniProtKB/Swiss-Prot),   E9PEM7 (UniProtKB/Swiss-Prot),   E5RFV9 (UniProtKB/Swiss-Prot),   B7Z4A2 (UniProtKB/Swiss-Prot),   B7Z496 (UniProtKB/Swiss-Prot),   B5KVR8 (UniProtKB/Swiss-Prot),   B5KVR6 (UniProtKB/Swiss-Prot),   Q96P82 (UniProtKB/Swiss-Prot),   Q9Y2G2 (UniProtKB/Swiss-Prot),   I6L9C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011524943   ⟸   XM_011526641
- Peptide Label: isoform X1
- UniProtKB: Q6PGP8 (UniProtKB/Swiss-Prot),   G3XAM9 (UniProtKB/Swiss-Prot),   E9PEM7 (UniProtKB/Swiss-Prot),   E5RFV9 (UniProtKB/Swiss-Prot),   B7Z4A2 (UniProtKB/Swiss-Prot),   B7Z496 (UniProtKB/Swiss-Prot),   B5KVR8 (UniProtKB/Swiss-Prot),   B5KVR6 (UniProtKB/Swiss-Prot),   Q96P82 (UniProtKB/Swiss-Prot),   Q9Y2G2 (UniProtKB/Swiss-Prot),   I6L9C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016881974   ⟸   XM_017026485
- Peptide Label: isoform X6
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016881971   ⟸   XM_017026482
- Peptide Label: isoform X2
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016881973   ⟸   XM_017026484
- Peptide Label: isoform X4
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016881972   ⟸   XM_017026483
- Peptide Label: isoform X3
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016881976   ⟸   XM_017026487
- Peptide Label: isoform X13
- UniProtKB: B5KVR7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001338716   ⟸   NM_001351787
- Peptide Label: isoform g
- Sequence:
RefSeq Acc Id: NP_001338720   ⟸   NM_001351791
- Peptide Label: isoform j
- Sequence:
RefSeq Acc Id: NP_001338717   ⟸   NM_001351788
- Peptide Label: isoform h
- Sequence:
RefSeq Acc Id: NP_001338715   ⟸   NM_001351786
- Peptide Label: isoform f
- UniProtKB: B5KVR7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001338718   ⟸   NM_001351789
- Peptide Label: isoform h
- Sequence:
RefSeq Acc Id: NP_001338721   ⟸   NM_001351792
- Peptide Label: isoform j
- Sequence:
RefSeq Acc Id: NP_001338713   ⟸   NM_001351784
- Peptide Label: isoform e
- UniProtKB: B5KVR7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001338719   ⟸   NM_001351790
- Peptide Label: isoform i
- Sequence:
RefSeq Acc Id: NP_001338711   ⟸   NM_001351782
- Peptide Label: isoform a
- UniProtKB: Q9Y2G2 (UniProtKB/Swiss-Prot),   Q6PGP8 (UniProtKB/Swiss-Prot),   G3XAM9 (UniProtKB/Swiss-Prot),   E9PEM7 (UniProtKB/Swiss-Prot),   E5RFV9 (UniProtKB/Swiss-Prot),   B7Z4A2 (UniProtKB/Swiss-Prot),   B7Z496 (UniProtKB/Swiss-Prot),   B5KVR8 (UniProtKB/Swiss-Prot),   B5KVR6 (UniProtKB/Swiss-Prot),   Q96P82 (UniProtKB/Swiss-Prot),   I6L9C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001338712   ⟸   NM_001351783
- Peptide Label: isoform b
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001352879   ⟸   NM_001365950
- Peptide Label: isoform k
- UniProtKB: B5KVR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: ENSP00000428662   ⟸   ENST00000517510
RefSeq Acc Id: ENSP00000430495   ⟸   ENST00000518979
RefSeq Acc Id: ENSP00000430057   ⟸   ENST00000518622
RefSeq Acc Id: ENSP00000428975   ⟸   ENST00000518450
RefSeq Acc Id: ENSP00000430108   ⟸   ENST00000519332
RefSeq Acc Id: ENSP00000429741   ⟸   ENST00000519302
RefSeq Acc Id: ENSP00000428883   ⟸   ENST00000519940
RefSeq Acc Id: ENSP00000430836   ⟸   ENST00000519646
RefSeq Acc Id: ENSP00000499211   ⟸   ENST00000651546
RefSeq Acc Id: ENSP00000430747   ⟸   ENST00000520015
RefSeq Acc Id: ENSP00000427727   ⟸   ENST00000520007
RefSeq Acc Id: ENSP00000428736   ⟸   ENST00000520153
RefSeq Acc Id: ENSP00000429839   ⟸   ENST00000520753
RefSeq Acc Id: ENSP00000427858   ⟸   ENST00000521613
RefSeq Acc Id: ENSP00000428862   ⟸   ENST00000521415
RefSeq Acc Id: ENSP00000430178   ⟸   ENST00000521437
RefSeq Acc Id: ENSP00000427922   ⟸   ENST00000522431
RefSeq Acc Id: ENSP00000430567   ⟸   ENST00000522889
RefSeq Acc Id: ENSP00000429362   ⟸   ENST00000522773
RefSeq Acc Id: ENSP00000430460   ⟸   ENST00000523579
RefSeq Acc Id: ENSP00000375767   ⟸   ENST00000391898
RefSeq Acc Id: ENSP00000391248   ⟸   ENST00000447740
RefSeq Acc Id: XP_047294411   ⟸   XM_047438455
- Peptide Label: isoform X6
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294417   ⟸   XM_047438461
- Peptide Label: isoform X12
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294409   ⟸   XM_047438453
- Peptide Label: isoform X5
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294410   ⟸   XM_047438454
- Peptide Label: isoform X5
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294419   ⟸   XM_047438463
- Peptide Label: isoform X16
RefSeq Acc Id: XP_047294403   ⟸   XM_047438447
- Peptide Label: isoform X3
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294393   ⟸   XM_047438437
- Peptide Label: isoform X1
- UniProtKB: Q9Y2G2 (UniProtKB/Swiss-Prot),   Q6PGP8 (UniProtKB/Swiss-Prot),   G3XAM9 (UniProtKB/Swiss-Prot),   E9PEM7 (UniProtKB/Swiss-Prot),   E5RFV9 (UniProtKB/Swiss-Prot),   B7Z4A2 (UniProtKB/Swiss-Prot),   B7Z496 (UniProtKB/Swiss-Prot),   B5KVR8 (UniProtKB/Swiss-Prot),   B5KVR6 (UniProtKB/Swiss-Prot),   Q96P82 (UniProtKB/Swiss-Prot),   I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294408   ⟸   XM_047438452
- Peptide Label: isoform X4
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294402   ⟸   XM_047438446
- Peptide Label: isoform X3
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294395   ⟸   XM_047438439
- Peptide Label: isoform X2
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294405   ⟸   XM_047438449
- Peptide Label: isoform X4
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294391   ⟸   XM_047438435
- Peptide Label: isoform X1
- UniProtKB: Q9Y2G2 (UniProtKB/Swiss-Prot),   Q6PGP8 (UniProtKB/Swiss-Prot),   G3XAM9 (UniProtKB/Swiss-Prot),   E9PEM7 (UniProtKB/Swiss-Prot),   E5RFV9 (UniProtKB/Swiss-Prot),   B7Z4A2 (UniProtKB/Swiss-Prot),   B7Z496 (UniProtKB/Swiss-Prot),   B5KVR8 (UniProtKB/Swiss-Prot),   B5KVR6 (UniProtKB/Swiss-Prot),   Q96P82 (UniProtKB/Swiss-Prot),   I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294401   ⟸   XM_047438445
- Peptide Label: isoform X3
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294397   ⟸   XM_047438441
- Peptide Label: isoform X2
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294392   ⟸   XM_047438436
- Peptide Label: isoform X1
- UniProtKB: Q9Y2G2 (UniProtKB/Swiss-Prot),   Q6PGP8 (UniProtKB/Swiss-Prot),   G3XAM9 (UniProtKB/Swiss-Prot),   E9PEM7 (UniProtKB/Swiss-Prot),   E5RFV9 (UniProtKB/Swiss-Prot),   B7Z4A2 (UniProtKB/Swiss-Prot),   B7Z496 (UniProtKB/Swiss-Prot),   B5KVR8 (UniProtKB/Swiss-Prot),   B5KVR6 (UniProtKB/Swiss-Prot),   Q96P82 (UniProtKB/Swiss-Prot),   I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294407   ⟸   XM_047438451
- Peptide Label: isoform X4
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294400   ⟸   XM_047438444
- Peptide Label: isoform X3
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294399   ⟸   XM_047438443
- Peptide Label: isoform X2
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294415   ⟸   XM_047438459
- Peptide Label: isoform X10
- UniProtKB: B5KVR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294406   ⟸   XM_047438450
- Peptide Label: isoform X4
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294394   ⟸   XM_047438438
- Peptide Label: isoform X1
- UniProtKB: Q9Y2G2 (UniProtKB/Swiss-Prot),   Q6PGP8 (UniProtKB/Swiss-Prot),   G3XAM9 (UniProtKB/Swiss-Prot),   E9PEM7 (UniProtKB/Swiss-Prot),   E5RFV9 (UniProtKB/Swiss-Prot),   B7Z4A2 (UniProtKB/Swiss-Prot),   B7Z496 (UniProtKB/Swiss-Prot),   B5KVR8 (UniProtKB/Swiss-Prot),   B5KVR6 (UniProtKB/Swiss-Prot),   Q96P82 (UniProtKB/Swiss-Prot),   I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294404   ⟸   XM_047438448
- Peptide Label: isoform X4
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294396   ⟸   XM_047438440
- Peptide Label: isoform X2
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294390   ⟸   XM_047438434
- Peptide Label: isoform X1
- UniProtKB: Q9Y2G2 (UniProtKB/Swiss-Prot),   Q6PGP8 (UniProtKB/Swiss-Prot),   G3XAM9 (UniProtKB/Swiss-Prot),   E9PEM7 (UniProtKB/Swiss-Prot),   E5RFV9 (UniProtKB/Swiss-Prot),   B7Z4A2 (UniProtKB/Swiss-Prot),   B7Z496 (UniProtKB/Swiss-Prot),   B5KVR8 (UniProtKB/Swiss-Prot),   B5KVR6 (UniProtKB/Swiss-Prot),   Q96P82 (UniProtKB/Swiss-Prot),   I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294398   ⟸   XM_047438442
- Peptide Label: isoform X2
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294414   ⟸   XM_047438458
- Peptide Label: isoform X9
- UniProtKB: B5KVR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294413   ⟸   XM_047438457
- Peptide Label: isoform X8
- UniProtKB: B5KVR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294412   ⟸   XM_047438456
- Peptide Label: isoform X7
- UniProtKB: B5KVR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294416   ⟸   XM_047438460
- Peptide Label: isoform X11
- UniProtKB: B5KVR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294421   ⟸   XM_047438465
- Peptide Label: isoform X18
RefSeq Acc Id: XP_047294418   ⟸   XM_047438462
- Peptide Label: isoform X15
RefSeq Acc Id: XP_047294420   ⟸   XM_047438464
- Peptide Label: isoform X17
RefSeq Acc Id: XP_054176236   ⟸   XM_054320261
- Peptide Label: isoform X6
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176237   ⟸   XM_054320262
- Peptide Label: isoform X6
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176241   ⟸   XM_054320266
- Peptide Label: isoform X12
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176234   ⟸   XM_054320259
- Peptide Label: isoform X5
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176235   ⟸   XM_054320260
- Peptide Label: isoform X5
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176243   ⟸   XM_054320268
- Peptide Label: isoform X14
RefSeq Acc Id: XP_054176245   ⟸   XM_054320270
- Peptide Label: isoform X16
RefSeq Acc Id: XP_054176226   ⟸   XM_054320251
- Peptide Label: isoform X3
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176212   ⟸   XM_054320237
- Peptide Label: isoform X1
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176233   ⟸   XM_054320258
- Peptide Label: isoform X4
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176222   ⟸   XM_054320247
- Peptide Label: isoform X3
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176218   ⟸   XM_054320243
- Peptide Label: isoform X2
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176210   ⟸   XM_054320235
- Peptide Label: isoform X1
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176225   ⟸   XM_054320250
- Peptide Label: isoform X3
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176214   ⟸   XM_054320239
- Peptide Label: isoform X1
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176224   ⟸   XM_054320249
- Peptide Label: isoform X3
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176228   ⟸   XM_054320253
- Peptide Label: isoform X4
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176215   ⟸   XM_054320240
- Peptide Label: isoform X2
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176230   ⟸   XM_054320255
- Peptide Label: isoform X4
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176227   ⟸   XM_054320252
- Peptide Label: isoform X3
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176207   ⟸   XM_054320232
- Peptide Label: isoform X1
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176209   ⟸   XM_054320234
- Peptide Label: isoform X1
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176223   ⟸   XM_054320248
- Peptide Label: isoform X3
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176217   ⟸   XM_054320242
- Peptide Label: isoform X2
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176211   ⟸   XM_054320236
- Peptide Label: isoform X1
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176232   ⟸   XM_054320257
- Peptide Label: isoform X4
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176221   ⟸   XM_054320246
- Peptide Label: isoform X3
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176220   ⟸   XM_054320245
- Peptide Label: isoform X2
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176231   ⟸   XM_054320256
- Peptide Label: isoform X4
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176208   ⟸   XM_054320233
- Peptide Label: isoform X1
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176213   ⟸   XM_054320238
- Peptide Label: isoform X1
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176229   ⟸   XM_054320254
- Peptide Label: isoform X4
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176216   ⟸   XM_054320241
- Peptide Label: isoform X2
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176206   ⟸   XM_054320231
- Peptide Label: isoform X1
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176219   ⟸   XM_054320244
- Peptide Label: isoform X2
- UniProtKB: I6L9C6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176240   ⟸   XM_054320265
- Peptide Label: isoform X19
- UniProtKB: B5KVR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176242   ⟸   XM_054320267
- Peptide Label: isoform X13
- UniProtKB: B5KVR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176239   ⟸   XM_054320264
- Peptide Label: isoform X11
- UniProtKB: B5KVR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176238   ⟸   XM_054320263
- Peptide Label: isoform X11
- UniProtKB: B5KVR7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176246   ⟸   XM_054320271
- Peptide Label: isoform X18
RefSeq Acc Id: XP_054176244   ⟸   XM_054320269
- Peptide Label: isoform X15
Protein Domains
CARD   FIIND

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9Y2G2-F1-model_v2 AlphaFold Q9Y2G2 1-537 view protein structure

Promoters
RGD ID:13204923
Promoter ID:EPDNEW_H26044
Type:initiation region
Name:CARD8_3
Description:caspase recruitment domain family member 8
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26045  EPDNEW_H26046  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,249,568 - 48,249,628EPDNEW
RGD ID:13204925
Promoter ID:EPDNEW_H26045
Type:initiation region
Name:CARD8_1
Description:caspase recruitment domain family member 8
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26044  EPDNEW_H26046  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,249,828 - 48,249,888EPDNEW
RGD ID:13204927
Promoter ID:EPDNEW_H26046
Type:initiation region
Name:CARD8_2
Description:caspase recruitment domain family member 8
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26044  EPDNEW_H26045  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381948,255,911 - 48,255,971EPDNEW
RGD ID:6795706
Promoter ID:HG_KWN:30429
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000357778,   ENST00000391898,   NM_001184901,   NM_001184903,   UC002PIE.2,   UC002PIF.2,   UC002PIG.2,   UC002PIH.2,   UC010ELT.1,   UC010ELU.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361953,444,594 - 53,445,094 (-)MPROMDB
RGD ID:6795245
Promoter ID:HG_KWN:30431
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   Lymphoblastoid
Transcripts:NM_001184904,   UC002PII.2
Position:
Human AssemblyChrPosition (strand)Source
Build 361953,450,634 - 53,451,134 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:17057 AgrOrtholog
COSMIC CARD8 COSMIC
Ensembl Genes ENSG00000105483 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000391898 ENTREZGENE
  ENST00000391898.7 UniProtKB/Swiss-Prot
  ENST00000447740 ENTREZGENE
  ENST00000447740.6 UniProtKB/Swiss-Prot
  ENST00000517510.5 UniProtKB/TrEMBL
  ENST00000518450.5 UniProtKB/TrEMBL
  ENST00000518622 ENTREZGENE
  ENST00000518622.5 UniProtKB/TrEMBL
  ENST00000518979.5 UniProtKB/TrEMBL
  ENST00000519302.6 UniProtKB/TrEMBL
  ENST00000519332 ENTREZGENE
  ENST00000519332.5 UniProtKB/Swiss-Prot
  ENST00000519646.5 UniProtKB/TrEMBL
  ENST00000519940 ENTREZGENE
  ENST00000519940.6 UniProtKB/Swiss-Prot
  ENST00000520007.5 UniProtKB/Swiss-Prot
  ENST00000520015 ENTREZGENE
  ENST00000520015.5 UniProtKB/Swiss-Prot
  ENST00000520153 ENTREZGENE
  ENST00000520153.5 UniProtKB/Swiss-Prot
  ENST00000520753 ENTREZGENE
  ENST00000520753.5 UniProtKB/Swiss-Prot
  ENST00000521415.5 UniProtKB/TrEMBL
  ENST00000521437.1 UniProtKB/TrEMBL
  ENST00000521613 ENTREZGENE
  ENST00000521613.5 UniProtKB/Swiss-Prot
  ENST00000522431.5 UniProtKB/Swiss-Prot
  ENST00000522773.5 UniProtKB/TrEMBL
  ENST00000522889.5 UniProtKB/TrEMBL
  ENST00000523579.5 UniProtKB/TrEMBL
  ENST00000651546 ENTREZGENE
  ENST00000651546.1 UniProtKB/Swiss-Prot
Gene3D-CATH 1.10.533.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000105483 GTEx
HGNC ID HGNC:17057 ENTREZGENE
Human Proteome Map CARD8 Human Proteome Map
InterPro CARD UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DEATH-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FIIND_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:22900 UniProtKB/Swiss-Prot
NCBI Gene 22900 ENTREZGENE
OMIM 609051 OMIM
PANTHER CASPASE RECRUITMENT DOMAIN-CONTAINING PROTEIN 8 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  NACHT, LRR AND PYD DOMAINS-CONTAINING PROTEIN 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam CARD UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FIIND UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134916154 PharmGKB
PROSITE CARD UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FIIND UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF47986 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt B5KVR6 ENTREZGENE
  B5KVR7 ENTREZGENE, UniProtKB/TrEMBL
  B5KVR8 ENTREZGENE
  B7Z496 ENTREZGENE
  B7Z4A2 ENTREZGENE
  CARD8_HUMAN UniProtKB/Swiss-Prot
  E5RFI5_HUMAN UniProtKB/TrEMBL
  E5RFV9 ENTREZGENE
  E5RGC9_HUMAN UniProtKB/TrEMBL
  E5RGG3_HUMAN UniProtKB/TrEMBL
  E5RHJ3_HUMAN UniProtKB/TrEMBL
  E5RHZ3_HUMAN UniProtKB/TrEMBL
  E5RIN1_HUMAN UniProtKB/TrEMBL
  E5RJG3_HUMAN UniProtKB/TrEMBL
  E9PEM7 ENTREZGENE
  G3XAM9 ENTREZGENE
  H0YB90_HUMAN UniProtKB/TrEMBL
  H0YBW7_HUMAN UniProtKB/TrEMBL
  I6L9C6 ENTREZGENE, UniProtKB/TrEMBL
  Q6PGP8 ENTREZGENE
  Q96P82 ENTREZGENE
  Q9Y2G2 ENTREZGENE
UniProt Secondary B5KVR6 UniProtKB/Swiss-Prot
  B5KVR8 UniProtKB/Swiss-Prot
  B7Z496 UniProtKB/Swiss-Prot
  B7Z4A2 UniProtKB/Swiss-Prot
  E5RFV9 UniProtKB/Swiss-Prot
  E9PEM7 UniProtKB/Swiss-Prot
  G3XAM9 UniProtKB/Swiss-Prot
  Q6PGP8 UniProtKB/Swiss-Prot
  Q96P82 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-11-24 CARD8  caspase recruitment domain family member 8    caspase recruitment domain family, member 8  Symbol and/or name change 5135510 APPROVED