Canonical Allele Identifier: CA1268208150

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575205T= , CM000664.2:g.88575205T=	GRCh38
NC_000002.11:g.88874723T= , CM000664.1:g.88874723T=	GRCh37
NC_000002.10:g.88655838T=	NCBI36
NG_016424.1:g.57372A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2106A=
ENST00000682276.1:n.1723A=
ENST00000682892.1:c.1825A=	ENSP00000507214.1:p.Asn609=
ENST00000682952.1:n.1917A=
ENST00000684455.1:c.1491A=
ENST00000684642.1:c.1675A=	ENSP00000507355.1:p.Asn559=
ENST00000684740.1:n.2456A=
ENST00000303236.9:c.2278A= MANE Select	ENSP00000307235.3:p.Asn760=
ENST00000652099.1:c.2472A=
ENST00000652736.1:n.2154A=
ENST00000303236.7:c.2278A=	ENSP00000307235.3:p.Asn760=
ENST00000415570.1:c.1915A=	ENSP00000412076.1:p.Asn639=
ENST00000419748.5:c.1825A=	ENSP00000408325.1:p.Asn609=
ENST00000470706.1:n.49-128A=
NM_001313915.1:c.1825A=	NP_001300844.1:p.Asn609=
NM_004836.5:c.2278A=	NP_004827.4:p.Asn760=
NM_004836.6:c.2278A=	NP_004827.4:p.Asn760=
NR_110236.1:n.1342T=
XM_005264649.3:c.1594A=	XP_005264706.1:p.Asn532=
XM_017005376.2:c.1594A=	XP_016860865.1:p.Asn532=
NM_004836.7:c.2278A= MANE Select	NP_004827.4:p.Asn760=
NM_001313915.2:c.1825A=	NP_001300844.1:p.Asn609=