Canonical Allele Identifier: CA1188220454

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737104_109737107delinsCTTG , CM000663.2:g.109737104_109737107delinsCTTG GRCh38
NC_000001.10:g.110279726_110279729delinsCTTG , CM000663.1:g.110279726_110279729delinsCTTG GRCh37
NC_000001.9:g.110081249_110081252delinsCTTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.642_645delinsCAAG (GSTM3) MANE Select ENSP00000354357.2:p.Asn214=
ENST00000256594.7:c.642_645delinsCAAG (GSTM3) ENSP00000256594.3:p.Asn214=
ENST00000361066.6:c.642_645delinsCAAG (GSTM3) ENSP00000354357.2:p.Asn214=
ENST00000429410.2:n.82+24756_82+24759delinsCTTG (GSTM5)
ENST00000476321.5:n.610_613delinsCAAG (GSTM3)
ENST00000486823.5:n.606_609delinsCAAG (GSTM3)
ENST00000488824.1:n.987_990delinsCAAG (GSTM3)
NM_000849.4:c.642_645delinsCAAG (GSTM3) NP_000840.2:p.Asn214=
NR_024537.1:n.876_879delinsCAAG (GSTM3)
XM_011541296.1:c.861_864delinsCAAG (GSTM3) XP_011539598.1:p.Asn287=
NM_000849.5:c.642_645delinsCAAG (GSTM3) MANE Select NP_000840.2:p.Asn214=
NR_024537.2:n.876_879delinsCAAG (GSTM3)