Canonical Allele Identifier: CA1268208158

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575228C= , CM000664.2:g.88575228C=	GRCh38
NC_000002.11:g.88874746C= , CM000664.1:g.88874746C=	GRCh37
NC_000002.10:g.88655861C=	NCBI36
NG_016424.1:g.57349G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2083G=
ENST00000682276.1:n.1700G=
ENST00000682892.1:c.1802G=	ENSP00000507214.1:p.Ser601=
ENST00000682952.1:n.1894G=
ENST00000684455.1:c.1468G=
ENST00000684642.1:c.1652G=	ENSP00000507355.1:p.Ser551=
ENST00000684740.1:n.2433G=
ENST00000303236.9:c.2255G= MANE Select	ENSP00000307235.3:p.Ser752=
ENST00000652099.1:c.2449G=
ENST00000652736.1:n.2131G=
ENST00000303236.7:c.2255G=	ENSP00000307235.3:p.Ser752=
ENST00000415570.1:c.1892G=	ENSP00000412076.1:p.Ser631=
ENST00000419748.5:c.1802G=	ENSP00000408325.1:p.Ser601=
ENST00000470706.1:n.48+133G=
NM_001313915.1:c.1802G=	NP_001300844.1:p.Ser601=
NM_004836.5:c.2255G=	NP_004827.4:p.Ser752=
NM_004836.6:c.2255G=	NP_004827.4:p.Ser752=
NR_110236.1:n.1365C=
XM_005264649.3:c.1571G=	XP_005264706.1:p.Ser524=
XM_017005376.2:c.1571G=	XP_016860865.1:p.Ser524=
NM_004836.7:c.2255G= MANE Select	NP_004827.4:p.Ser752=
NM_001313915.2:c.1802G=	NP_001300844.1:p.Ser601=