Canonical Allele Identifier: CA1268208088

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575020C= , CM000664.2:g.88575020C=	GRCh38
NC_000002.11:g.88874538C= , CM000664.1:g.88874538C=	GRCh37
NC_000002.10:g.88655653C=	NCBI36
NG_016424.1:g.57557G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2291G=
ENST00000682103.1:c.4G=
ENST00000682276.1:n.1908G=
ENST00000682892.1:c.2010G=	ENSP00000507214.1:p.Glu670=
ENST00000682952.1:n.2102G=
ENST00000684455.1:c.1676G=
ENST00000684642.1:c.1860G=	ENSP00000507355.1:p.Glu620=
ENST00000684740.1:n.2641G=
ENST00000303236.9:c.2463G= MANE Select	ENSP00000307235.3:p.Glu821=
ENST00000652099.1:c.2657G=
ENST00000652736.1:n.2339G=
ENST00000303236.7:c.2463G=	ENSP00000307235.3:p.Glu821=
ENST00000415570.1:c.2100G=	ENSP00000412076.1:p.Glu700=
ENST00000419748.5:c.2010G=	ENSP00000408325.1:p.Glu670=
ENST00000470706.1:n.106G=
NM_001313915.1:c.2010G=	NP_001300844.1:p.Glu670=
NM_004836.5:c.2463G=	NP_004827.4:p.Glu821=
NM_004836.6:c.2463G=	NP_004827.4:p.Glu821=
NR_110236.1:n.1157C=
XM_005264649.3:c.1779G=	XP_005264706.1:p.Glu593=
XM_017005376.2:c.1779G=	XP_016860865.1:p.Glu593=
NM_004836.7:c.2463G= MANE Select	NP_004827.4:p.Glu821=
NM_001313915.2:c.2010G=	NP_001300844.1:p.Glu670=