Canonical Allele Identifier: CA347592312
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575245C>G , CM000664.2:g.88575245C>G GRCh38
NC_000002.11:g.88874763C>G , CM000664.1:g.88874763C>G GRCh37
NC_000002.10:g.88655878C>G NCBI36
NG_016424.1:g.57332G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2066G>C
ENST00000682276.1:n.1683G>C
ENST00000682892.1:c.1785G>C ENSP00000507214.1:p.Met595Ile
ENST00000682952.1:n.1877G>C
ENST00000684455.1:c.1451G>C
ENST00000684642.1:c.1635G>C ENSP00000507355.1:p.Met545Ile
ENST00000684740.1:n.2416G>C
ENST00000303236.9:c.2238G>C MANE Select ENSP00000307235.3:p.Met746Ile
ENST00000652099.1:c.2432G>C
ENST00000652736.1:n.2114G>C
ENST00000303236.7:c.2238G>C ENSP00000307235.3:p.Met746Ile
ENST00000415570.1:c.1875G>C ENSP00000412076.1:p.Met625Ile
ENST00000419748.5:c.1785G>C ENSP00000408325.1:p.Met595Ile
ENST00000470706.1:n.48+116G>C
NM_001313915.1:c.1785G>C NP_001300844.1:p.Met595Ile
NM_004836.5:c.2238G>C NP_004827.4:p.Met746Ile
NM_004836.6:c.2238G>C NP_004827.4:p.Met746Ile
NR_110236.1:n.1382C>G
XM_005264649.3:c.1554G>C XP_005264706.1:p.Met518Ile
XM_017005376.2:c.1554G>C XP_016860865.1:p.Met518Ile
NM_004836.7:c.2238G>C MANE Select NP_004827.4:p.Met746Ile
NM_001313915.2:c.1785G>C NP_001300844.1:p.Met595Ile