Canonical Allele Identifier: CA347591689
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575111T>C , CM000664.2:g.88575111T>C GRCh38
NC_000002.11:g.88874629T>C , CM000664.1:g.88874629T>C GRCh37
NC_000002.10:g.88655744T>C NCBI36
NG_016424.1:g.57466A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2200A>G
ENST00000682276.1:n.1817A>G
ENST00000682892.1:c.1919A>G ENSP00000507214.1:p.Glu640Gly
ENST00000682952.1:n.2011A>G
ENST00000684455.1:c.1585A>G
ENST00000684642.1:c.1769A>G ENSP00000507355.1:p.Glu590Gly
ENST00000684740.1:n.2550A>G
ENST00000303236.9:c.2372A>G MANE Select ENSP00000307235.3:p.Glu791Gly
ENST00000652099.1:c.2566A>G
ENST00000652736.1:n.2248A>G
ENST00000303236.7:c.2372A>G ENSP00000307235.3:p.Glu791Gly
ENST00000415570.1:c.2009A>G ENSP00000412076.1:p.Glu670Gly
ENST00000419748.5:c.1919A>G ENSP00000408325.1:p.Glu640Gly
ENST00000470706.1:n.49-34A>G
NM_001313915.1:c.1919A>G NP_001300844.1:p.Glu640Gly
NM_004836.5:c.2372A>G NP_004827.4:p.Glu791Gly
NM_004836.6:c.2372A>G NP_004827.4:p.Glu791Gly
NR_110236.1:n.1248T>C
XM_005264649.3:c.1688A>G XP_005264706.1:p.Glu563Gly
XM_017005376.2:c.1688A>G XP_016860865.1:p.Glu563Gly
NM_004836.7:c.2372A>G MANE Select NP_004827.4:p.Glu791Gly
NM_001313915.2:c.1919A>G NP_001300844.1:p.Glu640Gly