Canonical Allele Identifier: CA347591302
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575024T>G , CM000664.2:g.88575024T>G GRCh38
NC_000002.11:g.88874542T>G , CM000664.1:g.88874542T>G GRCh37
NC_000002.10:g.88655657T>G NCBI36
NG_016424.1:g.57553A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2287A>C
ENST00000682276.1:n.1904A>C
ENST00000682892.1:c.2006A>C ENSP00000507214.1:p.Glu669Ala
ENST00000682952.1:n.2098A>C
ENST00000684455.1:c.1672A>C
ENST00000684642.1:c.1856A>C ENSP00000507355.1:p.Glu619Ala
ENST00000684740.1:n.2637A>C
ENST00000303236.9:c.2459A>C MANE Select ENSP00000307235.3:p.Glu820Ala
ENST00000652099.1:c.2653A>C
ENST00000652736.1:n.2335A>C
ENST00000303236.7:c.2459A>C ENSP00000307235.3:p.Glu820Ala
ENST00000415570.1:c.2096A>C ENSP00000412076.1:p.Glu699Ala
ENST00000419748.5:c.2006A>C ENSP00000408325.1:p.Glu669Ala
ENST00000470706.1:n.102A>C
NM_001313915.1:c.2006A>C NP_001300844.1:p.Glu669Ala
NM_004836.5:c.2459A>C NP_004827.4:p.Glu820Ala
NM_004836.6:c.2459A>C NP_004827.4:p.Glu820Ala
NR_110236.1:n.1161T>G
XM_005264649.3:c.1775A>C XP_005264706.1:p.Glu592Ala
XM_017005376.2:c.1775A>C XP_016860865.1:p.Glu592Ala
NM_004836.7:c.2459A>C MANE Select NP_004827.4:p.Glu820Ala
NM_001313915.2:c.2006A>C NP_001300844.1:p.Glu669Ala