Canonical Allele Identifier: CA1005674793

Linked Data

dbSNP Id: rs1649222829

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737137del , CM000663.2:g.109737137del GRCh38
NC_000001.10:g.110279759del , CM000663.1:g.110279759del GRCh37
NC_000001.9:g.110081282del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.612del (GSTM3) MANE Select ENSP00000354357.2:p.Asp205IlefsTer?
ENST00000256594.7:c.612del (GSTM3) ENSP00000256594.3:p.Asp205IlefsTer?
ENST00000361066.6:c.612del (GSTM3) ENSP00000354357.2:p.Asp205IlefsTer?
ENST00000429410.2:n.82+24789del (GSTM5)
ENST00000476321.5:n.580del (GSTM3)
ENST00000486823.5:n.576del (GSTM3)
ENST00000488824.1:n.957del (GSTM3)
NM_000849.4:c.612del (GSTM3) NP_000840.2:p.Asp205IlefsTer?
NR_024537.1:n.846del (GSTM3)
XM_011541296.1:c.831del (GSTM3) XP_011539598.1:p.Asp278IlefsTer?
NM_000849.5:c.612del (GSTM3) MANE Select NP_000840.2:p.Asp205IlefsTer?
NR_024537.2:n.846del (GSTM3)