Canonical Allele Identifier: CA1268208228

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575401T= , CM000664.2:g.88575401T=	GRCh38
NC_000002.11:g.88874919T= , CM000664.1:g.88874919T=	GRCh37
NC_000002.10:g.88656034T=	NCBI36
NG_016424.1:g.57176A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.1910A=
ENST00000682276.1:n.1527A=
ENST00000682892.1:c.1629A=	ENSP00000507214.1:p.Ser543=
ENST00000682952.1:n.1721A=
ENST00000684455.1:c.1295A=
ENST00000684642.1:c.1479A=	ENSP00000507355.1:p.Ser493=
ENST00000684740.1:n.2260A=
ENST00000303236.9:c.2082A= MANE Select	ENSP00000307235.3:p.Ser694=
ENST00000652099.1:c.2276A=
ENST00000652736.1:n.1958A=
ENST00000303236.7:c.2082A=	ENSP00000307235.3:p.Ser694=
ENST00000415570.1:c.1719A=	ENSP00000412076.1:p.Ser573=
ENST00000419748.5:c.1629A=	ENSP00000408325.1:p.Ser543=
ENST00000470706.1:n.8A=
ENST00000478003.1:n.648A=
NM_001313915.1:c.1629A=	NP_001300844.1:p.Ser543=
NM_004836.5:c.2082A=	NP_004827.4:p.Ser694=
NM_004836.6:c.2082A=	NP_004827.4:p.Ser694=
NR_110236.1:n.1538T=
XM_005264649.3:c.1398A=	XP_005264706.1:p.Ser466=
XR_939749.1:n.2361A=
XM_017005376.2:c.1398A=	XP_016860865.1:p.Ser466=
NM_004836.7:c.2082A= MANE Select	NP_004827.4:p.Ser694=
NM_001313915.2:c.1629A=	NP_001300844.1:p.Ser543=