Canonical Allele Identifier: CA347591724
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575119A>T , CM000664.2:g.88575119A>T GRCh38
NC_000002.11:g.88874637A>T , CM000664.1:g.88874637A>T GRCh37
NC_000002.10:g.88655752A>T NCBI36
NG_016424.1:g.57458T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2192T>A
ENST00000682276.1:n.1809T>A
ENST00000682892.1:c.1911T>A ENSP00000507214.1:p.Cys637Ter
ENST00000682952.1:n.2003T>A
ENST00000684455.1:c.1577T>A
ENST00000684642.1:c.1761T>A ENSP00000507355.1:p.Cys587Ter
ENST00000684740.1:n.2542T>A
ENST00000303236.9:c.2364T>A MANE Select ENSP00000307235.3:p.Cys788Ter
ENST00000652099.1:c.2558T>A
ENST00000652736.1:n.2240T>A
ENST00000303236.7:c.2364T>A ENSP00000307235.3:p.Cys788Ter
ENST00000415570.1:c.2001T>A ENSP00000412076.1:p.Cys667Ter
ENST00000419748.5:c.1911T>A ENSP00000408325.1:p.Cys637Ter
ENST00000470706.1:n.49-42T>A
NM_001313915.1:c.1911T>A NP_001300844.1:p.Cys637Ter
NM_004836.5:c.2364T>A NP_004827.4:p.Cys788Ter
NM_004836.6:c.2364T>A NP_004827.4:p.Cys788Ter
NR_110236.1:n.1256A>T
XM_005264649.3:c.1680T>A XP_005264706.1:p.Cys560Ter
XM_017005376.2:c.1680T>A XP_016860865.1:p.Cys560Ter
NM_004836.7:c.2364T>A MANE Select NP_004827.4:p.Cys788Ter
NM_001313915.2:c.1911T>A NP_001300844.1:p.Cys637Ter