Canonical Allele Identifier: CA2646987802

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737187_109737199del , CM000663.2:g.109737187_109737199del GRCh38
NC_000001.10:g.110279809_110279821del , CM000663.1:g.110279809_110279821del GRCh37
NC_000001.9:g.110081332_110081344del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.580-28_580-16del (GSTM3) MANE Select ENSP00000354357.2:n.580-28_580-16del
ENST00000256594.7:c.580-28_580-16del (GSTM3) ENSP00000256594.3:n.580-28_580-16del
ENST00000361066.6:c.580-28_580-16del (GSTM3) ENSP00000354357.2:n.580-28_580-16del
ENST00000429410.2:n.82+24839_82+24851del (GSTM5)
ENST00000476321.5:n.520_532del (GSTM3)
ENST00000486823.5:n.544-28_544-16del (GSTM3)
ENST00000488824.1:n.925-28_925-16del (GSTM3)
NM_000849.4:c.580-28_580-16del (GSTM3) NP_000840.2:n.580-28_580-16del
NR_024537.1:n.814-28_814-16del (GSTM3)
XM_011541296.1:c.799-28_799-16del (GSTM3) XP_011539598.1:n.799-28_799-16del
NM_000849.5:c.580-28_580-16del (GSTM3) MANE Select NP_000840.2:n.580-28_580-16del
NR_024537.2:n.814-28_814-16del (GSTM3)