Canonical Allele Identifier: CA1188220462

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737120A= , CM000663.2:g.109737120A= GRCh38
NC_000001.10:g.110279742A= , CM000663.1:g.110279742A= GRCh37
NC_000001.9:g.110081265A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.629T= (GSTM3) MANE Select ENSP00000354357.2:p.Met210=
ENST00000256594.7:c.629T= (GSTM3) ENSP00000256594.3:p.Met210=
ENST00000361066.6:c.629T= (GSTM3) ENSP00000354357.2:p.Met210=
ENST00000429410.2:n.82+24772A= (GSTM5)
ENST00000476321.5:n.597T= (GSTM3)
ENST00000486823.5:n.593T= (GSTM3)
ENST00000488824.1:n.974T= (GSTM3)
NM_000849.4:c.629T= (GSTM3) NP_000840.2:p.Met210=
NR_024537.1:n.863T= (GSTM3)
XM_011541296.1:c.848T= (GSTM3) XP_011539598.1:p.Met283=
NM_000849.5:c.629T= (GSTM3) MANE Select NP_000840.2:p.Met210=
NR_024537.2:n.863T= (GSTM3)