Canonical Allele Identifier: CA10636384

Gene: ADK

Linked Data

• ClinVar Variation Id: 300845
• ClinVar RCV Id: RCV000359874
• dbSNP Id: rs886047238
• gnomAD v3: 10-74708782-T-G
• gnomAD v4: 10-74708782-T-G
• MyVariant Identifiers: chr10:g.76468540T>G (hg19) ; chr10:g.74708782T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74708782T>G , CM000672.2:g.74708782T>G	GRCh38
NC_000010.10:g.76468540T>G , CM000672.1:g.76468540T>G	GRCh37
NC_000010.9:g.76138546T>G	NCBI36
NG_030484.1:g.562598T>G
NG_030484.2:g.562598T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000286621.7:c.*485T>G	ENSP00000286621.3:n.*485T>G
ENST00000372734.5:c.*337T>G	ENSP00000361819.3:n.*337T>G
ENST00000539909.6:c.*337T>G MANE Select	ENSP00000443965.2:n.*337T>G
ENST00000541550.6:c.*426T>G	ENSP00000438321.2:n.*426T>G
ENST00000673310.1:c.*1019T>G	ENSP00000500097.1:n.*1019T>G
ENST00000673352.1:c.*426T>G	ENSP00000500056.1:n.*426T>G
ENST00000372734.3:c.*337T>G	ENSP00000361819.3:n.*337T>G
ENST00000539909.5:c.*337T>G	ENSP00000443965.1:n.*337T>G
ENST00000541550.5:c.*337T>G	ENSP00000438321.1:n.*337T>G
NM_001123.3:c.*337T>G	NP_001114.2:n.*337T>G
NM_001202449.1:c.*337T>G	NP_001189378.1:n.*337T>G
NM_001202450.1:c.*337T>G	NP_001189379.1:n.*337T>G
NM_006721.3:c.*337T>G	NP_006712.2:n.*337T>G
XM_011539297.1:c.*337T>G	XP_011537599.1:n.*337T>G
XM_017015699.1:c.*337T>G	XP_016871188.1:n.*337T>G
XM_017015700.1:c.*426T>G	XP_016871189.1:n.*426T>G
XM_017015701.1:c.*337T>G	XP_016871190.1:n.*337T>G
XM_017015702.1:c.*426T>G	XP_016871191.1:n.*426T>G
XM_017015703.2:c.*337T>G	XP_016871192.1:n.*337T>G
XM_017015705.1:c.*426T>G	XP_016871194.1:n.*426T>G
NM_001369123.1:c.*426T>G	NP_001356052.1:n.*426T>G
NM_001369124.1:c.*337T>G	NP_001356053.1:n.*337T>G
NM_006721.4:c.*337T>G MANE Select	NP_006712.2:n.*337T>G
NM_001123.4:c.*337T>G	NP_001114.2:n.*337T>G
NM_001202449.2:c.*337T>G	NP_001189378.1:n.*337T>G
NM_001202450.2:c.*337T>G	NP_001189379.1:n.*337T>G