Canonical Allele Identifier: CA347591882
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575154C>G , CM000664.2:g.88575154C>G GRCh38
NC_000002.11:g.88874672C>G , CM000664.1:g.88874672C>G GRCh37
NC_000002.10:g.88655787C>G NCBI36
NG_016424.1:g.57423G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2157G>C
ENST00000682276.1:n.1774G>C
ENST00000682892.1:c.1876G>C ENSP00000507214.1:p.Asp626His
ENST00000682952.1:n.1968G>C
ENST00000684455.1:c.1542G>C
ENST00000684642.1:c.1726G>C ENSP00000507355.1:p.Asp576His
ENST00000684740.1:n.2507G>C
ENST00000303236.9:c.2329G>C MANE Select ENSP00000307235.3:p.Asp777His
ENST00000652099.1:c.2523G>C
ENST00000652736.1:n.2205G>C
ENST00000303236.7:c.2329G>C ENSP00000307235.3:p.Asp777His
ENST00000415570.1:c.1966G>C ENSP00000412076.1:p.Asp656His
ENST00000419748.5:c.1876G>C ENSP00000408325.1:p.Asp626His
ENST00000470706.1:n.49-77G>C
NM_001313915.1:c.1876G>C NP_001300844.1:p.Asp626His
NM_004836.5:c.2329G>C NP_004827.4:p.Asp777His
NM_004836.6:c.2329G>C NP_004827.4:p.Asp777His
NR_110236.1:n.1291C>G
XM_005264649.3:c.1645G>C XP_005264706.1:p.Asp549His
XM_017005376.2:c.1645G>C XP_016860865.1:p.Asp549His
NM_004836.7:c.2329G>C MANE Select NP_004827.4:p.Asp777His
NM_001313915.2:c.1876G>C NP_001300844.1:p.Asp626His