Canonical Allele Identifier: CA1268208137

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575163C= , CM000664.2:g.88575163C=	GRCh38
NC_000002.11:g.88874681C= , CM000664.1:g.88874681C=	GRCh37
NC_000002.10:g.88655796C=	NCBI36
NG_016424.1:g.57414G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2148G=
ENST00000682276.1:n.1765G=
ENST00000682892.1:c.1867G=	ENSP00000507214.1:p.Gly623=
ENST00000682952.1:n.1959G=
ENST00000684455.1:c.1533G=
ENST00000684642.1:c.1717G=	ENSP00000507355.1:p.Gly573=
ENST00000684740.1:n.2498G=
ENST00000303236.9:c.2320G= MANE Select	ENSP00000307235.3:p.Gly774=
ENST00000652099.1:c.2514G=
ENST00000652736.1:n.2196G=
ENST00000303236.7:c.2320G=	ENSP00000307235.3:p.Gly774=
ENST00000415570.1:c.1957G=	ENSP00000412076.1:p.Gly653=
ENST00000419748.5:c.1867G=	ENSP00000408325.1:p.Gly623=
ENST00000470706.1:n.49-86G=
NM_001313915.1:c.1867G=	NP_001300844.1:p.Gly623=
NM_004836.5:c.2320G=	NP_004827.4:p.Gly774=
NM_004836.6:c.2320G=	NP_004827.4:p.Gly774=
NR_110236.1:n.1300C=
XM_005264649.3:c.1636G=	XP_005264706.1:p.Gly546=
XM_017005376.2:c.1636G=	XP_016860865.1:p.Gly546=
NM_004836.7:c.2320G= MANE Select	NP_004827.4:p.Gly774=
NM_001313915.2:c.1867G=	NP_001300844.1:p.Gly623=