Canonical Allele Identifier: CA1268208102

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575058C= , CM000664.2:g.88575058C=	GRCh38
NC_000002.11:g.88874576C= , CM000664.1:g.88874576C=	GRCh37
NC_000002.10:g.88655691C=	NCBI36
NG_016424.1:g.57519G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2253G=
ENST00000682276.1:n.1870G=
ENST00000682892.1:c.1972G=	ENSP00000507214.1:p.Glu658=
ENST00000682952.1:n.2064G=
ENST00000684455.1:c.1638G=
ENST00000684642.1:c.1822G=	ENSP00000507355.1:p.Glu608=
ENST00000684740.1:n.2603G=
ENST00000303236.9:c.2425G= MANE Select	ENSP00000307235.3:p.Glu809=
ENST00000652099.1:c.2619G=
ENST00000652736.1:n.2301G=
ENST00000303236.7:c.2425G=	ENSP00000307235.3:p.Glu809=
ENST00000415570.1:c.2062G=	ENSP00000412076.1:p.Glu688=
ENST00000419748.5:c.1972G=	ENSP00000408325.1:p.Glu658=
ENST00000470706.1:n.68G=
NM_001313915.1:c.1972G=	NP_001300844.1:p.Glu658=
NM_004836.5:c.2425G=	NP_004827.4:p.Glu809=
NM_004836.6:c.2425G=	NP_004827.4:p.Glu809=
NR_110236.1:n.1195C=
XM_005264649.3:c.1741G=	XP_005264706.1:p.Glu581=
XM_017005376.2:c.1741G=	XP_016860865.1:p.Glu581=
NM_004836.7:c.2425G= MANE Select	NP_004827.4:p.Glu809=
NM_001313915.2:c.1972G=	NP_001300844.1:p.Glu658=