Canonical Allele Identifier: CA347591446

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874575T>A (hg19) ; chr2:g.88575057T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575057T>A , CM000664.2:g.88575057T>A	GRCh38
NC_000002.11:g.88874575T>A , CM000664.1:g.88874575T>A	GRCh37
NC_000002.10:g.88655690T>A	NCBI36
NG_016424.1:g.57520A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2254A>T
ENST00000682276.1:n.1871A>T
ENST00000682892.1:c.1973A>T	ENSP00000507214.1:p.Glu658Val
ENST00000682952.1:n.2065A>T
ENST00000684455.1:c.1639A>T
ENST00000684642.1:c.1823A>T	ENSP00000507355.1:p.Glu608Val
ENST00000684740.1:n.2604A>T
ENST00000303236.9:c.2426A>T MANE Select	ENSP00000307235.3:p.Glu809Val
ENST00000652099.1:c.2620A>T
ENST00000652736.1:n.2302A>T
ENST00000303236.7:c.2426A>T	ENSP00000307235.3:p.Glu809Val
ENST00000415570.1:c.2063A>T	ENSP00000412076.1:p.Glu688Val
ENST00000419748.5:c.1973A>T	ENSP00000408325.1:p.Glu658Val
ENST00000470706.1:n.69A>T
NM_001313915.1:c.1973A>T	NP_001300844.1:p.Glu658Val
NM_004836.5:c.2426A>T	NP_004827.4:p.Glu809Val
NM_004836.6:c.2426A>T	NP_004827.4:p.Glu809Val
NR_110236.1:n.1194T>A
XM_005264649.3:c.1742A>T	XP_005264706.1:p.Glu581Val
XM_017005376.2:c.1742A>T	XP_016860865.1:p.Glu581Val
NM_004836.7:c.2426A>T MANE Select	NP_004827.4:p.Glu809Val
NM_001313915.2:c.1973A>T	NP_001300844.1:p.Glu658Val