Canonical Allele Identifier: CA1268208226

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575397T= , CM000664.2:g.88575397T=	GRCh38
NC_000002.11:g.88874915T= , CM000664.1:g.88874915T=	GRCh37
NC_000002.10:g.88656030T=	NCBI36
NG_016424.1:g.57180A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.1914A=
ENST00000682276.1:n.1531A=
ENST00000682892.1:c.1633A=	ENSP00000507214.1:p.Lys545=
ENST00000682952.1:n.1725A=
ENST00000684455.1:c.1299A=
ENST00000684642.1:c.1483A=	ENSP00000507355.1:p.Lys495=
ENST00000684740.1:n.2264A=
ENST00000303236.9:c.2086A= MANE Select	ENSP00000307235.3:p.Lys696=
ENST00000652099.1:c.2280A=
ENST00000652736.1:n.1962A=
ENST00000303236.7:c.2086A=	ENSP00000307235.3:p.Lys696=
ENST00000415570.1:c.1723A=	ENSP00000412076.1:p.Lys575=
ENST00000419748.5:c.1633A=	ENSP00000408325.1:p.Lys545=
ENST00000470706.1:n.12A=
ENST00000478003.1:n.652A=
NM_001313915.1:c.1633A=	NP_001300844.1:p.Lys545=
NM_004836.5:c.2086A=	NP_004827.4:p.Lys696=
NM_004836.6:c.2086A=	NP_004827.4:p.Lys696=
NR_110236.1:n.1534T=
XM_005264649.3:c.1402A=	XP_005264706.1:p.Lys468=
XR_939749.1:n.2365A=
XM_017005376.2:c.1402A=	XP_016860865.1:p.Lys468=
NM_004836.7:c.2086A= MANE Select	NP_004827.4:p.Lys696=
NM_001313915.2:c.1633A=	NP_001300844.1:p.Lys545=