Canonical Allele Identifier: CA1188220569

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737367A= , CM000663.2:g.109737367A= GRCh38
NC_000001.10:g.110279989A= , CM000663.1:g.110279989A= GRCh37
NC_000001.9:g.110081512A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.579+90T= (GSTM3) MANE Select ENSP00000354357.2:n.579+90T=
ENST00000256594.7:c.579+90T= (GSTM3) ENSP00000256594.3:n.579+90T=
ENST00000361066.6:c.579+90T= (GSTM3) ENSP00000354357.2:n.579+90T=
ENST00000429410.2:n.82+25019A= (GSTM5)
ENST00000476321.5:n.350T= (GSTM3)
ENST00000486823.5:n.543+90T= (GSTM3)
ENST00000488824.1:n.924+90T= (GSTM3)
ENST00000540225.2:c.*20T= (GSTM3) ENSP00000444978.2:n.*20T=
NM_000849.4:c.579+90T= (GSTM3) NP_000840.2:n.579+90T=
NR_024537.1:n.813+90T= (GSTM3)
XM_011541296.1:c.798+90T= (GSTM3) XP_011539598.1:n.798+90T=
NM_000849.5:c.579+90T= (GSTM3) MANE Select NP_000840.2:n.579+90T=
NR_024537.2:n.813+90T= (GSTM3)