Canonical Allele Identifier: CA1268208237

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575428G= , CM000664.2:g.88575428G=	GRCh38
NC_000002.11:g.88874946G= , CM000664.1:g.88874946G=	GRCh37
NC_000002.10:g.88656061G=	NCBI36
NG_016424.1:g.57149C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.1883C=
ENST00000682276.1:n.1500C=
ENST00000682892.1:c.1602C=	ENSP00000507214.1:p.Ser534=
ENST00000682952.1:n.1694C=
ENST00000684455.1:c.1268C=
ENST00000684642.1:c.1452C=	ENSP00000507355.1:p.Ser484=
ENST00000684740.1:n.2233C=
ENST00000303236.9:c.2055C= MANE Select	ENSP00000307235.3:p.Ser685=
ENST00000652099.1:c.2249C=
ENST00000652736.1:n.1931C=
ENST00000303236.7:c.2055C=	ENSP00000307235.3:p.Ser685=
ENST00000415570.1:c.1692C=	ENSP00000412076.1:p.Ser564=
ENST00000419748.5:c.1602C=	ENSP00000408325.1:p.Ser534=
ENST00000478003.1:n.621C=
NM_001313915.1:c.1602C=	NP_001300844.1:p.Ser534=
NM_004836.5:c.2055C=	NP_004827.4:p.Ser685=
NM_004836.6:c.2055C=	NP_004827.4:p.Ser685=
NR_110236.1:n.1565G=
XM_005264649.3:c.1371C=	XP_005264706.1:p.Ser457=
XR_939749.1:n.2334C=
XM_017005376.2:c.1371C=	XP_016860865.1:p.Ser457=
NM_004836.7:c.2055C= MANE Select	NP_004827.4:p.Ser685=
NM_001313915.2:c.1602C=	NP_001300844.1:p.Ser534=