Canonical Allele Identifier: CA347591459
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575059A>C , CM000664.2:g.88575059A>C GRCh38
NC_000002.11:g.88874577A>C , CM000664.1:g.88874577A>C GRCh37
NC_000002.10:g.88655692A>C NCBI36
NG_016424.1:g.57518T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2252T>G
ENST00000682276.1:n.1869T>G
ENST00000682892.1:c.1971T>G ENSP00000507214.1:p.Phe657Leu
ENST00000682952.1:n.2063T>G
ENST00000684455.1:c.1637T>G
ENST00000684642.1:c.1821T>G ENSP00000507355.1:p.Phe607Leu
ENST00000684740.1:n.2602T>G
ENST00000303236.9:c.2424T>G MANE Select ENSP00000307235.3:p.Phe808Leu
ENST00000652099.1:c.2618T>G
ENST00000652736.1:n.2300T>G
ENST00000303236.7:c.2424T>G ENSP00000307235.3:p.Phe808Leu
ENST00000415570.1:c.2061T>G ENSP00000412076.1:p.Phe687Leu
ENST00000419748.5:c.1971T>G ENSP00000408325.1:p.Phe657Leu
ENST00000470706.1:n.67T>G
NM_001313915.1:c.1971T>G NP_001300844.1:p.Phe657Leu
NM_004836.5:c.2424T>G NP_004827.4:p.Phe808Leu
NM_004836.6:c.2424T>G NP_004827.4:p.Phe808Leu
NR_110236.1:n.1196A>C
XM_005264649.3:c.1740T>G XP_005264706.1:p.Phe580Leu
XM_017005376.2:c.1740T>G XP_016860865.1:p.Phe580Leu
NM_004836.7:c.2424T>G MANE Select NP_004827.4:p.Phe808Leu
NM_001313915.2:c.1971T>G NP_001300844.1:p.Phe657Leu