Canonical Allele Identifier: CA2646987711

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737093dup , CM000663.2:g.109737093dup GRCh38
NC_000001.10:g.110279715dup , CM000663.1:g.110279715dup GRCh37
NC_000001.9:g.110081238dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361066.7:c.659dup (GSTM3) MANE Select ENSP00000354357.2:p.Asn221GlnfsTer22
ENST00000256594.7:c.659dup (GSTM3) ENSP00000256594.3:p.Asn221GlnfsTer22
ENST00000361066.6:c.659dup (GSTM3) ENSP00000354357.2:p.Asn221GlnfsTer22
ENST00000429410.2:n.82+24745dup (GSTM5)
ENST00000476321.5:n.627dup (GSTM3)
ENST00000486823.5:n.623dup (GSTM3)
ENST00000488824.1:n.1004dup (GSTM3)
NM_000849.4:c.659dup (GSTM3) NP_000840.2:p.Asn221GlnfsTer22
NR_024537.1:n.893dup (GSTM3)
XM_011541296.1:c.878dup (GSTM3) XP_011539598.1:p.Asn294GlnfsTer22
NM_000849.5:c.659dup (GSTM3) MANE Select NP_000840.2:p.Asn221GlnfsTer22
NR_024537.2:n.893dup (GSTM3)