Canonical Allele Identifier: CA152717
Community Standard Title: NM_004836.7(EIF2AK3):c.497A>G (p.Gln166Arg)
Gene: EIF2AK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88595605T>C , CM000664.2:g.88595605T>C GRCh38
NC_000002.11:g.88895123T>C , CM000664.1:g.88895123T>C GRCh37
NC_000002.10:g.88676238T>C NCBI36
NG_016424.1:g.36972A>G

Transcript Alleles

HGVS Amino-acid Change
NM_004836.7:c.497A>G MANE Select NP_004827.4:p.Gln166Arg
ENST00000303236.9:c.497A>G MANE Select ENSP00000307235.3:p.Gln166Arg
NM_001313915.1:c.44A>G NP_001300844.1:p.Gln15Arg
NM_001313915.2:c.44A>G NP_001300844.1:p.Gln15Arg
NM_004836.5:c.497A>G NP_004827.4:p.Gln166Arg
NM_004836.6:c.497A>G NP_004827.4:p.Gln166Arg
ENST00000303236.7:c.497A>G ENSP00000307235.3:p.Gln166Arg
ENST00000415570.1:c.134A>G ENSP00000412076.1:p.Gln45Arg
ENST00000419748.5:c.44A>G ENSP00000408325.1:p.Gln15Arg
ENST00000652099.1:c.495A>G
ENST00000652736.1:n.373A>G
ENST00000682892.1:c.44A>G ENSP00000507214.1:p.Gln15Arg
XM_017005376.2:c.-384A>G XP_016860865.1:n.-384A>G
XR_939749.1:n.706A>G