Canonical Allele Identifier: CA1268208162

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575238C= , CM000664.2:g.88575238C=	GRCh38
NC_000002.11:g.88874756C= , CM000664.1:g.88874756C=	GRCh37
NC_000002.10:g.88655871C=	NCBI36
NG_016424.1:g.57339G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2073G=
ENST00000682276.1:n.1690G=
ENST00000682892.1:c.1792G=	ENSP00000507214.1:p.Glu598=
ENST00000682952.1:n.1884G=
ENST00000684455.1:c.1458G=
ENST00000684642.1:c.1642G=	ENSP00000507355.1:p.Glu548=
ENST00000684740.1:n.2423G=
ENST00000303236.9:c.2245G= MANE Select	ENSP00000307235.3:p.Glu749=
ENST00000652099.1:c.2439G=
ENST00000652736.1:n.2121G=
ENST00000303236.7:c.2245G=	ENSP00000307235.3:p.Glu749=
ENST00000415570.1:c.1882G=	ENSP00000412076.1:p.Glu628=
ENST00000419748.5:c.1792G=	ENSP00000408325.1:p.Glu598=
ENST00000470706.1:n.48+123G=
NM_001313915.1:c.1792G=	NP_001300844.1:p.Glu598=
NM_004836.5:c.2245G=	NP_004827.4:p.Glu749=
NM_004836.6:c.2245G=	NP_004827.4:p.Glu749=
NR_110236.1:n.1375C=
XM_005264649.3:c.1561G=	XP_005264706.1:p.Glu521=
XM_017005376.2:c.1561G=	XP_016860865.1:p.Glu521=
NM_004836.7:c.2245G= MANE Select	NP_004827.4:p.Glu749=
NM_001313915.2:c.1792G=	NP_001300844.1:p.Glu598=