Canonical Allele Identifier: CA1920147000

Gene: ADK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74708876G= , CM000672.2:g.74708876G=	GRCh38
NC_000010.10:g.76468634G= , CM000672.1:g.76468634G=	GRCh37
NC_000010.9:g.76138640G=	NCBI36
NG_030484.1:g.562692G=
NG_030484.2:g.562692G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372734.5:c.*431G=	ENSP00000361819.3:n.*431G=
ENST00000539909.6:c.*431G= MANE Select	ENSP00000443965.2:n.*431G=
ENST00000541550.6:c.*520G=	ENSP00000438321.2:n.*520G=
ENST00000673310.1:c.*1113G=	ENSP00000500097.1:n.*1113G=
ENST00000673352.1:c.*520G=	ENSP00000500056.1:n.*520G=
ENST00000372734.3:c.*431G=	ENSP00000361819.3:n.*431G=
ENST00000539909.5:c.*431G=	ENSP00000443965.1:n.*431G=
ENST00000541550.5:c.*431G=	ENSP00000438321.1:n.*431G=
NM_001123.3:c.*431G=	NP_001114.2:n.*431G=
NM_001202449.1:c.*431G=	NP_001189378.1:n.*431G=
NM_001202450.1:c.*431G=	NP_001189379.1:n.*431G=
NM_006721.3:c.*431G=	NP_006712.2:n.*431G=
XM_011539297.1:c.*431G=	XP_011537599.1:n.*431G=
XM_017015699.1:c.*431G=	XP_016871188.1:n.*431G=
XM_017015700.1:c.*520G=	XP_016871189.1:n.*520G=
XM_017015701.1:c.*431G=	XP_016871190.1:n.*431G=
XM_017015702.1:c.*520G=	XP_016871191.1:n.*520G=
XM_017015703.2:c.*431G=	XP_016871192.1:n.*431G=
XM_017015705.1:c.*520G=	XP_016871194.1:n.*520G=
NM_001369123.1:c.*520G=	NP_001356052.1:n.*520G=
NM_001369124.1:c.*431G=	NP_001356053.1:n.*431G=
NM_006721.4:c.*431G= MANE Select	NP_006712.2:n.*431G=
NM_001123.4:c.*431G=	NP_001114.2:n.*431G=
NM_001202449.2:c.*431G=	NP_001189378.1:n.*431G=
NM_001202450.2:c.*431G=	NP_001189379.1:n.*431G=