Canonical Allele Identifier: CA347591338
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575033G>C , CM000664.2:g.88575033G>C GRCh38
NC_000002.11:g.88874551G>C , CM000664.1:g.88874551G>C GRCh37
NC_000002.10:g.88655666G>C NCBI36
NG_016424.1:g.57544C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2278C>G
ENST00000682276.1:n.1895C>G
ENST00000682892.1:c.1997C>G ENSP00000507214.1:p.Ser666Cys
ENST00000682952.1:n.2089C>G
ENST00000684455.1:c.1663C>G
ENST00000684642.1:c.1847C>G ENSP00000507355.1:p.Ser616Cys
ENST00000684740.1:n.2628C>G
ENST00000303236.9:c.2450C>G MANE Select ENSP00000307235.3:p.Ser817Cys
ENST00000652099.1:c.2644C>G
ENST00000652736.1:n.2326C>G
ENST00000303236.7:c.2450C>G ENSP00000307235.3:p.Ser817Cys
ENST00000415570.1:c.2087C>G ENSP00000412076.1:p.Ser696Cys
ENST00000419748.5:c.1997C>G ENSP00000408325.1:p.Ser666Cys
ENST00000470706.1:n.93C>G
NM_001313915.1:c.1997C>G NP_001300844.1:p.Ser666Cys
NM_004836.5:c.2450C>G NP_004827.4:p.Ser817Cys
NM_004836.6:c.2450C>G NP_004827.4:p.Ser817Cys
NR_110236.1:n.1170G>C
XM_005264649.3:c.1766C>G XP_005264706.1:p.Ser589Cys
XM_017005376.2:c.1766C>G XP_016860865.1:p.Ser589Cys
NM_004836.7:c.2450C>G MANE Select NP_004827.4:p.Ser817Cys
NM_001313915.2:c.1997C>G NP_001300844.1:p.Ser666Cys