Canonical Allele Identifier: CA1268208136

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575159G= , CM000664.2:g.88575159G=	GRCh38
NC_000002.11:g.88874677G= , CM000664.1:g.88874677G=	GRCh37
NC_000002.10:g.88655792G=	NCBI36
NG_016424.1:g.57418C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2152C=
ENST00000682276.1:n.1769C=
ENST00000682892.1:c.1871C=	ENSP00000507214.1:p.Thr624=
ENST00000682952.1:n.1963C=
ENST00000684455.1:c.1537C=
ENST00000684642.1:c.1721C=	ENSP00000507355.1:p.Thr574=
ENST00000684740.1:n.2502C=
ENST00000303236.9:c.2324C= MANE Select	ENSP00000307235.3:p.Thr775=
ENST00000652099.1:c.2518C=
ENST00000652736.1:n.2200C=
ENST00000303236.7:c.2324C=	ENSP00000307235.3:p.Thr775=
ENST00000415570.1:c.1961C=	ENSP00000412076.1:p.Thr654=
ENST00000419748.5:c.1871C=	ENSP00000408325.1:p.Thr624=
ENST00000470706.1:n.49-82C=
NM_001313915.1:c.1871C=	NP_001300844.1:p.Thr624=
NM_004836.5:c.2324C=	NP_004827.4:p.Thr775=
NM_004836.6:c.2324C=	NP_004827.4:p.Thr775=
NR_110236.1:n.1296G=
XM_005264649.3:c.1640C=	XP_005264706.1:p.Thr547=
XM_017005376.2:c.1640C=	XP_016860865.1:p.Thr547=
NM_004836.7:c.2324C= MANE Select	NP_004827.4:p.Thr775=
NM_001313915.2:c.1871C=	NP_001300844.1:p.Thr624=