Canonical Allele Identifier: CA347591757
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575126T>C , CM000664.2:g.88575126T>C GRCh38
NC_000002.11:g.88874644T>C , CM000664.1:g.88874644T>C GRCh37
NC_000002.10:g.88655759T>C NCBI36
NG_016424.1:g.57451A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2185A>G
ENST00000682276.1:n.1802A>G
ENST00000682892.1:c.1904A>G ENSP00000507214.1:p.Glu635Gly
ENST00000682952.1:n.1996A>G
ENST00000684455.1:c.1570A>G
ENST00000684642.1:c.1754A>G ENSP00000507355.1:p.Glu585Gly
ENST00000684740.1:n.2535A>G
ENST00000303236.9:c.2357A>G MANE Select ENSP00000307235.3:p.Glu786Gly
ENST00000652099.1:c.2551A>G
ENST00000652736.1:n.2233A>G
ENST00000303236.7:c.2357A>G ENSP00000307235.3:p.Glu786Gly
ENST00000415570.1:c.1994A>G ENSP00000412076.1:p.Glu665Gly
ENST00000419748.5:c.1904A>G ENSP00000408325.1:p.Glu635Gly
ENST00000470706.1:n.49-49A>G
NM_001313915.1:c.1904A>G NP_001300844.1:p.Glu635Gly
NM_004836.5:c.2357A>G NP_004827.4:p.Glu786Gly
NM_004836.6:c.2357A>G NP_004827.4:p.Glu786Gly
NR_110236.1:n.1263T>C
XM_005264649.3:c.1673A>G XP_005264706.1:p.Glu558Gly
XM_017005376.2:c.1673A>G XP_016860865.1:p.Glu558Gly
NM_004836.7:c.2357A>G MANE Select NP_004827.4:p.Glu786Gly
NM_001313915.2:c.1904A>G NP_001300844.1:p.Glu635Gly