Canonical Allele Identifier: CA1268208182

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575304A= , CM000664.2:g.88575304A=	GRCh38
NC_000002.11:g.88874822A= , CM000664.1:g.88874822A=	GRCh37
NC_000002.10:g.88655937A=	NCBI36
NG_016424.1:g.57273T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2007T=
ENST00000682276.1:n.1624T=
ENST00000682892.1:c.1726T=	ENSP00000507214.1:p.Ser576=
ENST00000682952.1:n.1818T=
ENST00000684455.1:c.1392T=
ENST00000684642.1:c.1576T=	ENSP00000507355.1:p.Ser526=
ENST00000684740.1:n.2357T=
ENST00000303236.9:c.2179T= MANE Select	ENSP00000307235.3:p.Ser727=
ENST00000652099.1:c.2373T=
ENST00000652736.1:n.2055T=
ENST00000303236.7:c.2179T=	ENSP00000307235.3:p.Ser727=
ENST00000415570.1:c.1816T=	ENSP00000412076.1:p.Ser606=
ENST00000419748.5:c.1726T=	ENSP00000408325.1:p.Ser576=
ENST00000470706.1:n.48+57T=
NM_001313915.1:c.1726T=	NP_001300844.1:p.Ser576=
NM_004836.5:c.2179T=	NP_004827.4:p.Ser727=
NM_004836.6:c.2179T=	NP_004827.4:p.Ser727=
NR_110236.1:n.1441A=
XM_005264649.3:c.1495T=	XP_005264706.1:p.Ser499=
XR_939749.1:n.2458T=
XM_017005376.2:c.1495T=	XP_016860865.1:p.Ser499=
NM_004836.7:c.2179T= MANE Select	NP_004827.4:p.Ser727=
NM_001313915.2:c.1726T=	NP_001300844.1:p.Ser576=