Canonical Allele Identifier: CA341535917

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737165A>T , CM000663.2:g.109737165A>T GRCh38
NC_000001.10:g.110279787A>T , CM000663.1:g.110279787A>T GRCh37
NC_000001.9:g.110081310A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.584T>A (GSTM3) MANE Select ENSP00000354357.2:p.Leu195Ter
ENST00000256594.7:c.584T>A (GSTM3) ENSP00000256594.3:p.Leu195Ter
ENST00000361066.6:c.584T>A (GSTM3) ENSP00000354357.2:p.Leu195Ter
ENST00000429410.2:n.82+24817A>T (GSTM5)
ENST00000476321.5:n.552T>A (GSTM3)
ENST00000486823.5:n.548T>A (GSTM3)
ENST00000488824.1:n.929T>A (GSTM3)
NM_000849.4:c.584T>A (GSTM3) NP_000840.2:p.Leu195Ter
NR_024537.1:n.818T>A (GSTM3)
XM_011541296.1:c.803T>A (GSTM3) XP_011539598.1:p.Leu268Ter
NM_000849.5:c.584T>A (GSTM3) MANE Select NP_000840.2:p.Leu195Ter
NR_024537.2:n.818T>A (GSTM3)