Canonical Allele Identifier: CA347591404
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575048C>T , CM000664.2:g.88575048C>T GRCh38
NC_000002.11:g.88874566C>T , CM000664.1:g.88874566C>T GRCh37
NC_000002.10:g.88655681C>T NCBI36
NG_016424.1:g.57529G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2263G>A
ENST00000682276.1:n.1880G>A
ENST00000682892.1:c.1982G>A ENSP00000507214.1:p.Gly661Asp
ENST00000682952.1:n.2074G>A
ENST00000684455.1:c.1648G>A
ENST00000684642.1:c.1832G>A ENSP00000507355.1:p.Gly611Asp
ENST00000684740.1:n.2613G>A
ENST00000303236.9:c.2435G>A MANE Select ENSP00000307235.3:p.Gly812Asp
ENST00000652099.1:c.2629G>A
ENST00000652736.1:n.2311G>A
ENST00000303236.7:c.2435G>A ENSP00000307235.3:p.Gly812Asp
ENST00000415570.1:c.2072G>A ENSP00000412076.1:p.Gly691Asp
ENST00000419748.5:c.1982G>A ENSP00000408325.1:p.Gly661Asp
ENST00000470706.1:n.78G>A
NM_001313915.1:c.1982G>A NP_001300844.1:p.Gly661Asp
NM_004836.5:c.2435G>A NP_004827.4:p.Gly812Asp
NM_004836.6:c.2435G>A NP_004827.4:p.Gly812Asp
NR_110236.1:n.1185C>T
XM_005264649.3:c.1751G>A XP_005264706.1:p.Gly584Asp
XM_017005376.2:c.1751G>A XP_016860865.1:p.Gly584Asp
NM_004836.7:c.2435G>A MANE Select NP_004827.4:p.Gly812Asp
NM_001313915.2:c.1982G>A NP_001300844.1:p.Gly661Asp