Canonical Allele Identifier: CA1268208133

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575149G= , CM000664.2:g.88575149G=	GRCh38
NC_000002.11:g.88874667G= , CM000664.1:g.88874667G=	GRCh37
NC_000002.10:g.88655782G=	NCBI36
NG_016424.1:g.57428C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2162C=
ENST00000682276.1:n.1779C=
ENST00000682892.1:c.1881C=	ENSP00000507214.1:p.Gly627=
ENST00000682952.1:n.1973C=
ENST00000684455.1:c.1547C=
ENST00000684642.1:c.1731C=	ENSP00000507355.1:p.Gly577=
ENST00000684740.1:n.2512C=
ENST00000303236.9:c.2334C= MANE Select	ENSP00000307235.3:p.Gly778=
ENST00000652099.1:c.2528C=
ENST00000652736.1:n.2210C=
ENST00000303236.7:c.2334C=	ENSP00000307235.3:p.Gly778=
ENST00000415570.1:c.1971C=	ENSP00000412076.1:p.Gly657=
ENST00000419748.5:c.1881C=	ENSP00000408325.1:p.Gly627=
ENST00000470706.1:n.49-72C=
NM_001313915.1:c.1881C=	NP_001300844.1:p.Gly627=
NM_004836.5:c.2334C=	NP_004827.4:p.Gly778=
NM_004836.6:c.2334C=	NP_004827.4:p.Gly778=
NR_110236.1:n.1286G=
XM_005264649.3:c.1650C=	XP_005264706.1:p.Gly550=
XM_017005376.2:c.1650C=	XP_016860865.1:p.Gly550=
NM_004836.7:c.2334C= MANE Select	NP_004827.4:p.Gly778=
NM_001313915.2:c.1881C=	NP_001300844.1:p.Gly627=