Canonical Allele Identifier: CA1188220494

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737201A= , CM000663.2:g.109737201A= GRCh38
NC_000001.10:g.110279823A= , CM000663.1:g.110279823A= GRCh37
NC_000001.9:g.110081346A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.580-32T= (GSTM3) MANE Select ENSP00000354357.2:n.580-32T=
ENST00000256594.7:c.580-32T= (GSTM3) ENSP00000256594.3:n.580-32T=
ENST00000361066.6:c.580-32T= (GSTM3) ENSP00000354357.2:n.580-32T=
ENST00000429410.2:n.82+24853A= (GSTM5)
ENST00000476321.5:n.516T= (GSTM3)
ENST00000486823.5:n.544-32T= (GSTM3)
ENST00000488824.1:n.925-32T= (GSTM3)
NM_000849.4:c.580-32T= (GSTM3) NP_000840.2:n.580-32T=
NR_024537.1:n.814-32T= (GSTM3)
XM_011541296.1:c.799-32T= (GSTM3) XP_011539598.1:n.799-32T=
NM_000849.5:c.580-32T= (GSTM3) MANE Select NP_000840.2:n.580-32T=
NR_024537.2:n.814-32T= (GSTM3)