Canonical Allele Identifier: CA347591684
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575110T>A , CM000664.2:g.88575110T>A GRCh38
NC_000002.11:g.88874628T>A , CM000664.1:g.88874628T>A GRCh37
NC_000002.10:g.88655743T>A NCBI36
NG_016424.1:g.57467A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2201A>T
ENST00000682276.1:n.1818A>T
ENST00000682892.1:c.1920A>T ENSP00000507214.1:p.Glu640Asp
ENST00000682952.1:n.2012A>T
ENST00000684455.1:c.1586A>T
ENST00000684642.1:c.1770A>T ENSP00000507355.1:p.Glu590Asp
ENST00000684740.1:n.2551A>T
ENST00000303236.9:c.2373A>T MANE Select ENSP00000307235.3:p.Glu791Asp
ENST00000652099.1:c.2567A>T
ENST00000652736.1:n.2249A>T
ENST00000303236.7:c.2373A>T ENSP00000307235.3:p.Glu791Asp
ENST00000415570.1:c.2010A>T ENSP00000412076.1:p.Glu670Asp
ENST00000419748.5:c.1920A>T ENSP00000408325.1:p.Glu640Asp
ENST00000470706.1:n.49-33A>T
NM_001313915.1:c.1920A>T NP_001300844.1:p.Glu640Asp
NM_004836.5:c.2373A>T NP_004827.4:p.Glu791Asp
NM_004836.6:c.2373A>T NP_004827.4:p.Glu791Asp
NR_110236.1:n.1247T>A
XM_005264649.3:c.1689A>T XP_005264706.1:p.Glu563Asp
XM_017005376.2:c.1689A>T XP_016860865.1:p.Glu563Asp
NM_004836.7:c.2373A>T MANE Select NP_004827.4:p.Glu791Asp
NM_001313915.2:c.1920A>T NP_001300844.1:p.Glu640Asp