Canonical Allele Identifier: CA885397498

Linked Data

dbSNP Id: rs1204061173

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737143dup , CM000663.2:g.109737143dup GRCh38
NC_000001.10:g.110279765dup , CM000663.1:g.110279765dup GRCh37
NC_000001.9:g.110081288dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.606dup (GSTM3) MANE Select ENSP00000354357.2:p.Gln203ThrfsTer3
ENST00000256594.7:c.606dup (GSTM3) ENSP00000256594.3:p.Gln203ThrfsTer3
ENST00000361066.6:c.606dup (GSTM3) ENSP00000354357.2:p.Gln203ThrfsTer3
ENST00000429410.2:n.82+24795dup (GSTM5)
ENST00000476321.5:n.574dup (GSTM3)
ENST00000486823.5:n.570dup (GSTM3)
ENST00000488824.1:n.951dup (GSTM3)
NM_000849.4:c.606dup (GSTM3) NP_000840.2:p.Gln203ThrfsTer3
NR_024537.1:n.840dup (GSTM3)
XM_011541296.1:c.825dup (GSTM3) XP_011539598.1:p.Gln276ThrfsTer3
NM_000849.5:c.606dup (GSTM3) MANE Select NP_000840.2:p.Gln203ThrfsTer3
NR_024537.2:n.840dup (GSTM3)