Canonical Allele Identifier: CA470254867

Gene: ADK

Linked Data

• MyVariant Identifiers: chr10:g.76285184A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74525426A>C , CM000672.2:g.74525426A>C	GRCh38
NC_000010.10:g.76285184A>C , CM000672.1:g.76285184A>C	GRCh37
NC_000010.9:g.75955190A>C	NCBI36
NG_030484.1:g.379242A>C
NG_030484.2:g.379242A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286621.7:c.726A>C	ENSP00000286621.3:p.Thr242=
ENST00000372734.5:c.675A>C	ENSP00000361819.3:p.Thr225=
ENST00000539909.6:c.726A>C MANE Select	ENSP00000443965.2:p.Thr242=
ENST00000541550.6:c.675A>C	ENSP00000438321.2:p.Thr225=
ENST00000672394.1:c.450A>C	ENSP00000500390.1:p.Thr150=
ENST00000672429.1:c.556-63856A>C	ENSP00000500292.1:n.556-63856A>C
ENST00000672604.1:c.466A>C
ENST00000672920.1:c.*471A>C	ENSP00000500141.1:n.*471A>C
ENST00000673027.1:c.621A>C	ENSP00000500201.1:p.Thr207=
ENST00000673310.1:c.675A>C	ENSP00000500097.1:p.Thr225=
ENST00000673352.1:c.726A>C	ENSP00000500056.1:p.Thr242=
ENST00000286621.6:c.726A>C	ENSP00000286621.2:p.Thr242=
ENST00000372734.3:c.675A>C	ENSP00000361819.3:p.Thr225=
ENST00000467840.1:n.63A>C
ENST00000539909.5:c.556-63856A>C	ENSP00000443965.1:n.556-63856A>C
ENST00000541550.5:c.621A>C	ENSP00000438321.1:p.Thr207=
NM_001123.3:c.675A>C	NP_001114.2:p.Thr225=
NM_001202449.1:c.621A>C	NP_001189378.1:p.Thr207=
NM_001202450.1:c.556-63856A>C	NP_001189379.1:n.556-63856A>C
NM_006721.3:c.726A>C	NP_006712.2:p.Thr242=
NR_120673.1:n.259+2340T>G
XM_011539297.1:c.642A>C	XP_011537599.1:p.Thr214=
XM_017015698.1:c.726A>C	XP_016871187.1:p.Thr242=
XM_017015699.1:c.531A>C	XP_016871188.1:p.Thr177=
XM_017015700.1:c.726A>C	XP_016871189.1:p.Thr242=
XM_017015701.1:c.505-63856A>C	XP_016871190.1:n.505-63856A>C
XM_017015702.1:c.675A>C	XP_016871191.1:p.Thr225=
XM_017015703.2:c.450A>C	XP_016871192.1:p.Thr150=
XM_017015704.1:c.726A>C	XP_016871193.1:p.Thr242=
XM_017015705.1:c.556-63856A>C	XP_016871194.1:n.556-63856A>C
XM_017015706.1:c.675A>C	XP_016871195.1:p.Thr225=
NM_001369123.1:c.726A>C	NP_001356052.1:p.Thr242=
NM_001369124.1:c.505-63856A>C	NP_001356053.1:n.505-63856A>C
NM_006721.4:c.726A>C MANE Select	NP_006712.2:p.Thr242=
NM_001123.4:c.675A>C	NP_001114.2:p.Thr225=
NM_001202449.2:c.621A>C	NP_001189378.1:p.Thr207=
NM_001202450.2:c.556-63856A>C	NP_001189379.1:n.556-63856A>C