Canonical Allele Identifier: CA347592787
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575354T>A , CM000664.2:g.88575354T>A GRCh38
NC_000002.11:g.88874872T>A , CM000664.1:g.88874872T>A GRCh37
NC_000002.10:g.88655987T>A NCBI36
NG_016424.1:g.57223A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.1957A>T
ENST00000682276.1:n.1574A>T
ENST00000682892.1:c.1676A>T ENSP00000507214.1:p.Glu559Val
ENST00000682952.1:n.1768A>T
ENST00000684455.1:c.1342A>T
ENST00000684642.1:c.1526A>T ENSP00000507355.1:p.Glu509Val
ENST00000684740.1:n.2307A>T
ENST00000303236.9:c.2129A>T MANE Select ENSP00000307235.3:p.Glu710Val
ENST00000652099.1:c.2323A>T
ENST00000652736.1:n.2005A>T
ENST00000303236.7:c.2129A>T ENSP00000307235.3:p.Glu710Val
ENST00000415570.1:c.1766A>T ENSP00000412076.1:p.Glu589Val
ENST00000419748.5:c.1676A>T ENSP00000408325.1:p.Glu559Val
ENST00000470706.1:n.48+7A>T
NM_001313915.1:c.1676A>T NP_001300844.1:p.Glu559Val
NM_004836.5:c.2129A>T NP_004827.4:p.Glu710Val
NM_004836.6:c.2129A>T NP_004827.4:p.Glu710Val
NR_110236.1:n.1491T>A
XM_005264649.3:c.1445A>T XP_005264706.1:p.Glu482Val
XR_939749.1:n.2408A>T
XM_017005376.2:c.1445A>T XP_016860865.1:p.Glu482Val
NM_004836.7:c.2129A>T MANE Select NP_004827.4:p.Glu710Val
NM_001313915.2:c.1676A>T NP_001300844.1:p.Glu559Val