Canonical Allele Identifier: CA347591281
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575021T>G , CM000664.2:g.88575021T>G GRCh38
NC_000002.11:g.88874539T>G , CM000664.1:g.88874539T>G GRCh37
NC_000002.10:g.88655654T>G NCBI36
NG_016424.1:g.57556A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2290A>C
ENST00000682103.1:c.3A>C
ENST00000682276.1:n.1907A>C
ENST00000682892.1:c.2009A>C ENSP00000507214.1:p.Glu670Ala
ENST00000682952.1:n.2101A>C
ENST00000684455.1:c.1675A>C
ENST00000684642.1:c.1859A>C ENSP00000507355.1:p.Glu620Ala
ENST00000684740.1:n.2640A>C
ENST00000303236.9:c.2462A>C MANE Select ENSP00000307235.3:p.Glu821Ala
ENST00000652099.1:c.2656A>C
ENST00000652736.1:n.2338A>C
ENST00000303236.7:c.2462A>C ENSP00000307235.3:p.Glu821Ala
ENST00000415570.1:c.2099A>C ENSP00000412076.1:p.Glu700Ala
ENST00000419748.5:c.2009A>C ENSP00000408325.1:p.Glu670Ala
ENST00000470706.1:n.105A>C
NM_001313915.1:c.2009A>C NP_001300844.1:p.Glu670Ala
NM_004836.5:c.2462A>C NP_004827.4:p.Glu821Ala
NM_004836.6:c.2462A>C NP_004827.4:p.Glu821Ala
NR_110236.1:n.1158T>G
XM_005264649.3:c.1778A>C XP_005264706.1:p.Glu593Ala
XM_017005376.2:c.1778A>C XP_016860865.1:p.Glu593Ala
NM_004836.7:c.2462A>C MANE Select NP_004827.4:p.Glu821Ala
NM_001313915.2:c.2009A>C NP_001300844.1:p.Glu670Ala