Canonical Allele Identifier: CA347591685
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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