Canonical Allele Identifier: CA347591313
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575027T>G , CM000664.2:g.88575027T>G GRCh38
NC_000002.11:g.88874545T>G , CM000664.1:g.88874545T>G GRCh37
NC_000002.10:g.88655660T>G NCBI36
NG_016424.1:g.57550A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2284A>C
ENST00000682276.1:n.1901A>C
ENST00000682892.1:c.2003A>C ENSP00000507214.1:p.Lys668Thr
ENST00000682952.1:n.2095A>C
ENST00000684455.1:c.1669A>C
ENST00000684642.1:c.1853A>C ENSP00000507355.1:p.Lys618Thr
ENST00000684740.1:n.2634A>C
ENST00000303236.9:c.2456A>C MANE Select ENSP00000307235.3:p.Lys819Thr
ENST00000652099.1:c.2650A>C
ENST00000652736.1:n.2332A>C
ENST00000303236.7:c.2456A>C ENSP00000307235.3:p.Lys819Thr
ENST00000415570.1:c.2093A>C ENSP00000412076.1:p.Lys698Thr
ENST00000419748.5:c.2003A>C ENSP00000408325.1:p.Lys668Thr
ENST00000470706.1:n.99A>C
NM_001313915.1:c.2003A>C NP_001300844.1:p.Lys668Thr
NM_004836.5:c.2456A>C NP_004827.4:p.Lys819Thr
NM_004836.6:c.2456A>C NP_004827.4:p.Lys819Thr
NR_110236.1:n.1164T>G
XM_005264649.3:c.1772A>C XP_005264706.1:p.Lys591Thr
XM_017005376.2:c.1772A>C XP_016860865.1:p.Lys591Thr
NM_004836.7:c.2456A>C MANE Select NP_004827.4:p.Lys819Thr
NM_001313915.2:c.2003A>C NP_001300844.1:p.Lys668Thr