Canonical Allele Identifier: CA1268208084

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575016T= , CM000664.2:g.88575016T=	GRCh38
NC_000002.11:g.88874534T= , CM000664.1:g.88874534T=	GRCh37
NC_000002.10:g.88655649T=	NCBI36
NG_016424.1:g.57561A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2295A=
ENST00000682103.1:c.8A=
ENST00000682276.1:n.1912A=
ENST00000682892.1:c.2014A=	ENSP00000507214.1:p.Lys672=
ENST00000682952.1:n.2106A=
ENST00000684455.1:c.1680A=
ENST00000684642.1:c.1864A=	ENSP00000507355.1:p.Lys622=
ENST00000684740.1:n.2645A=
ENST00000303236.9:c.2467A= MANE Select	ENSP00000307235.3:p.Lys823=
ENST00000652099.1:c.2661A=
ENST00000652736.1:n.2343A=
ENST00000303236.7:c.2467A=	ENSP00000307235.3:p.Lys823=
ENST00000415570.1:c.2104A=	ENSP00000412076.1:p.Lys702=
ENST00000419748.5:c.2014A=	ENSP00000408325.1:p.Lys672=
ENST00000470706.1:n.110A=
NM_001313915.1:c.2014A=	NP_001300844.1:p.Lys672=
NM_004836.5:c.2467A=	NP_004827.4:p.Lys823=
NM_004836.6:c.2467A=	NP_004827.4:p.Lys823=
NR_110236.1:n.1153T=
XM_005264649.3:c.1783A=	XP_005264706.1:p.Lys595=
XM_017005376.2:c.1783A=	XP_016860865.1:p.Lys595=
NM_004836.7:c.2467A= MANE Select	NP_004827.4:p.Lys823=
NM_001313915.2:c.2014A=	NP_001300844.1:p.Lys672=