Canonical Allele Identifier: CA1268208169

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575248T= , CM000664.2:g.88575248T=	GRCh38
NC_000002.11:g.88874766T= , CM000664.1:g.88874766T=	GRCh37
NC_000002.10:g.88655881T=	NCBI36
NG_016424.1:g.57329A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2063A=
ENST00000682276.1:n.1680A=
ENST00000682892.1:c.1782A=	ENSP00000507214.1:p.Gly594=
ENST00000682952.1:n.1874A=
ENST00000684455.1:c.1448A=
ENST00000684642.1:c.1632A=	ENSP00000507355.1:p.Gly544=
ENST00000684740.1:n.2413A=
ENST00000303236.9:c.2235A= MANE Select	ENSP00000307235.3:p.Gly745=
ENST00000652099.1:c.2429A=
ENST00000652736.1:n.2111A=
ENST00000303236.7:c.2235A=	ENSP00000307235.3:p.Gly745=
ENST00000415570.1:c.1872A=	ENSP00000412076.1:p.Gly624=
ENST00000419748.5:c.1782A=	ENSP00000408325.1:p.Gly594=
ENST00000470706.1:n.48+113A=
NM_001313915.1:c.1782A=	NP_001300844.1:p.Gly594=
NM_004836.5:c.2235A=	NP_004827.4:p.Gly745=
NM_004836.6:c.2235A=	NP_004827.4:p.Gly745=
NR_110236.1:n.1385T=
XM_005264649.3:c.1551A=	XP_005264706.1:p.Gly517=
XM_017005376.2:c.1551A=	XP_016860865.1:p.Gly517=
NM_004836.7:c.2235A= MANE Select	NP_004827.4:p.Gly745=
NM_001313915.2:c.1782A=	NP_001300844.1:p.Gly594=