Canonical Allele Identifier: CA347593033
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575439A>T , CM000664.2:g.88575439A>T GRCh38
NC_000002.11:g.88874957A>T , CM000664.1:g.88874957A>T GRCh37
NC_000002.10:g.88656072A>T NCBI36
NG_016424.1:g.57138T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.1872T>A
ENST00000682276.1:n.1489T>A
ENST00000682892.1:c.1591T>A ENSP00000507214.1:p.Trp531Arg
ENST00000682952.1:n.1683T>A
ENST00000684455.1:c.1257T>A
ENST00000684642.1:c.1441T>A ENSP00000507355.1:p.Trp481Arg
ENST00000684740.1:n.2222T>A
ENST00000303236.9:c.2044T>A MANE Select ENSP00000307235.3:p.Trp682Arg
ENST00000652099.1:c.2238T>A
ENST00000652736.1:n.1920T>A
ENST00000303236.7:c.2044T>A ENSP00000307235.3:p.Trp682Arg
ENST00000415570.1:c.1681T>A ENSP00000412076.1:p.Trp561Arg
ENST00000419748.5:c.1591T>A ENSP00000408325.1:p.Trp531Arg
ENST00000478003.1:n.610T>A
NM_001313915.1:c.1591T>A NP_001300844.1:p.Trp531Arg
NM_004836.5:c.2044T>A NP_004827.4:p.Trp682Arg
NM_004836.6:c.2044T>A NP_004827.4:p.Trp682Arg
NR_110236.1:n.1576A>T
XM_005264649.3:c.1360T>A XP_005264706.1:p.Trp454Arg
XR_939749.1:n.2323T>A
XM_017005376.2:c.1360T>A XP_016860865.1:p.Trp454Arg
NM_004836.7:c.2044T>A MANE Select NP_004827.4:p.Trp682Arg
NM_001313915.2:c.1591T>A NP_001300844.1:p.Trp531Arg