Canonical Allele Identifier: CA1268208122

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575125T= , CM000664.2:g.88575125T=	GRCh38
NC_000002.11:g.88874643T= , CM000664.1:g.88874643T=	GRCh37
NC_000002.10:g.88655758T=	NCBI36
NG_016424.1:g.57452A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2186A=
ENST00000682276.1:n.1803A=
ENST00000682892.1:c.1905A=	ENSP00000507214.1:p.Glu635=
ENST00000682952.1:n.1997A=
ENST00000684455.1:c.1571A=
ENST00000684642.1:c.1755A=	ENSP00000507355.1:p.Glu585=
ENST00000684740.1:n.2536A=
ENST00000303236.9:c.2358A= MANE Select	ENSP00000307235.3:p.Glu786=
ENST00000652099.1:c.2552A=
ENST00000652736.1:n.2234A=
ENST00000303236.7:c.2358A=	ENSP00000307235.3:p.Glu786=
ENST00000415570.1:c.1995A=	ENSP00000412076.1:p.Glu665=
ENST00000419748.5:c.1905A=	ENSP00000408325.1:p.Glu635=
ENST00000470706.1:n.49-48A=
NM_001313915.1:c.1905A=	NP_001300844.1:p.Glu635=
NM_004836.5:c.2358A=	NP_004827.4:p.Glu786=
NM_004836.6:c.2358A=	NP_004827.4:p.Glu786=
NR_110236.1:n.1262T=
XM_005264649.3:c.1674A=	XP_005264706.1:p.Glu558=
XM_017005376.2:c.1674A=	XP_016860865.1:p.Glu558=
NM_004836.7:c.2358A= MANE Select	NP_004827.4:p.Glu786=
NM_001313915.2:c.1905A=	NP_001300844.1:p.Glu635=