Canonical Allele Identifier: CA1268208132

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575148T= , CM000664.2:g.88575148T=	GRCh38
NC_000002.11:g.88874666T= , CM000664.1:g.88874666T=	GRCh37
NC_000002.10:g.88655781T=	NCBI36
NG_016424.1:g.57429A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2163A=
ENST00000682276.1:n.1780A=
ENST00000682892.1:c.1882A=	ENSP00000507214.1:p.Asn628=
ENST00000682952.1:n.1974A=
ENST00000684455.1:c.1548A=
ENST00000684642.1:c.1732A=	ENSP00000507355.1:p.Asn578=
ENST00000684740.1:n.2513A=
ENST00000303236.9:c.2335A= MANE Select	ENSP00000307235.3:p.Asn779=
ENST00000652099.1:c.2529A=
ENST00000652736.1:n.2211A=
ENST00000303236.7:c.2335A=	ENSP00000307235.3:p.Asn779=
ENST00000415570.1:c.1972A=	ENSP00000412076.1:p.Asn658=
ENST00000419748.5:c.1882A=	ENSP00000408325.1:p.Asn628=
ENST00000470706.1:n.49-71A=
NM_001313915.1:c.1882A=	NP_001300844.1:p.Asn628=
NM_004836.5:c.2335A=	NP_004827.4:p.Asn779=
NM_004836.6:c.2335A=	NP_004827.4:p.Asn779=
NR_110236.1:n.1285T=
XM_005264649.3:c.1651A=	XP_005264706.1:p.Asn551=
XM_017005376.2:c.1651A=	XP_016860865.1:p.Asn551=
NM_004836.7:c.2335A= MANE Select	NP_004827.4:p.Asn779=
NM_001313915.2:c.1882A=	NP_001300844.1:p.Asn628=