Canonical Allele Identifier: CA1188220577

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737392G= , CM000663.2:g.109737392G= GRCh38
NC_000001.10:g.110280014G= , CM000663.1:g.110280014G= GRCh37
NC_000001.9:g.110081537G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.579+65C= (GSTM3) MANE Select ENSP00000354357.2:n.579+65C=
ENST00000256594.7:c.579+65C= (GSTM3) ENSP00000256594.3:n.579+65C=
ENST00000361066.6:c.579+65C= (GSTM3) ENSP00000354357.2:n.579+65C=
ENST00000429410.2:n.82+25044G= (GSTM5)
ENST00000476321.5:n.325C= (GSTM3)
ENST00000486823.5:n.543+65C= (GSTM3)
ENST00000488824.1:n.924+65C= (GSTM3)
ENST00000540225.2:c.634C= (GSTM3) ENSP00000444978.2:p.Pro212=
NM_000849.4:c.579+65C= (GSTM3) NP_000840.2:n.579+65C=
NR_024537.1:n.813+65C= (GSTM3)
XM_011541296.1:c.798+65C= (GSTM3) XP_011539598.1:n.798+65C=
NM_000849.5:c.579+65C= (GSTM3) MANE Select NP_000840.2:n.579+65C=
NR_024537.2:n.813+65C= (GSTM3)