Canonical Allele Identifier: CA1268208106

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575078G= , CM000664.2:g.88575078G=	GRCh38
NC_000002.11:g.88874596G= , CM000664.1:g.88874596G=	GRCh37
NC_000002.10:g.88655711G=	NCBI36
NG_016424.1:g.57499C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2233C=
ENST00000682276.1:n.1850C=
ENST00000682892.1:c.1952C=	ENSP00000507214.1:p.Thr651=
ENST00000682952.1:n.2044C=
ENST00000684455.1:c.1618C=
ENST00000684642.1:c.1802C=	ENSP00000507355.1:p.Thr601=
ENST00000684740.1:n.2583C=
ENST00000303236.9:c.2405C= MANE Select	ENSP00000307235.3:p.Thr802=
ENST00000652099.1:c.2599C=
ENST00000652736.1:n.2281C=
ENST00000303236.7:c.2405C=	ENSP00000307235.3:p.Thr802=
ENST00000415570.1:c.2042C=	ENSP00000412076.1:p.Thr681=
ENST00000419748.5:c.1952C=	ENSP00000408325.1:p.Thr651=
ENST00000470706.1:n.49-1C=
NM_001313915.1:c.1952C=	NP_001300844.1:p.Thr651=
NM_004836.5:c.2405C=	NP_004827.4:p.Thr802=
NM_004836.6:c.2405C=	NP_004827.4:p.Thr802=
NR_110236.1:n.1215G=
XM_005264649.3:c.1721C=	XP_005264706.1:p.Thr574=
XM_017005376.2:c.1721C=	XP_016860865.1:p.Thr574=
NM_004836.7:c.2405C= MANE Select	NP_004827.4:p.Thr802=
NM_001313915.2:c.1952C=	NP_001300844.1:p.Thr651=