Canonical Allele Identifier: CA1268208093

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575038A= , CM000664.2:g.88575038A=	GRCh38
NC_000002.11:g.88874556A= , CM000664.1:g.88874556A=	GRCh37
NC_000002.10:g.88655671A=	NCBI36
NG_016424.1:g.57539T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2273T=
ENST00000682276.1:n.1890T=
ENST00000682892.1:c.1992T=	ENSP00000507214.1:p.Asn664=
ENST00000682952.1:n.2084T=
ENST00000684455.1:c.1658T=
ENST00000684642.1:c.1842T=	ENSP00000507355.1:p.Asn614=
ENST00000684740.1:n.2623T=
ENST00000303236.9:c.2445T= MANE Select	ENSP00000307235.3:p.Asn815=
ENST00000652099.1:c.2639T=
ENST00000652736.1:n.2321T=
ENST00000303236.7:c.2445T=	ENSP00000307235.3:p.Asn815=
ENST00000415570.1:c.2082T=	ENSP00000412076.1:p.Asn694=
ENST00000419748.5:c.1992T=	ENSP00000408325.1:p.Asn664=
ENST00000470706.1:n.88T=
NM_001313915.1:c.1992T=	NP_001300844.1:p.Asn664=
NM_004836.5:c.2445T=	NP_004827.4:p.Asn815=
NM_004836.6:c.2445T=	NP_004827.4:p.Asn815=
NR_110236.1:n.1175A=
XM_005264649.3:c.1761T=	XP_005264706.1:p.Asn587=
XM_017005376.2:c.1761T=	XP_016860865.1:p.Asn587=
NM_004836.7:c.2445T= MANE Select	NP_004827.4:p.Asn815=
NM_001313915.2:c.1992T=	NP_001300844.1:p.Asn664=