Canonical Allele Identifier: CA2646987572

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737010dup , CM000663.2:g.109737010dup GRCh38
NC_000001.10:g.110279632dup , CM000663.1:g.110279632dup GRCh37
NC_000001.9:g.110081155dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*62dup (GSTM3) MANE Select ENSP00000354357.2:n.*62dup
ENST00000256594.7:c.*62dup (GSTM3) ENSP00000256594.3:n.*62dup
ENST00000361066.6:c.*62dup (GSTM3) ENSP00000354357.2:n.*62dup
ENST00000429410.2:n.82+24662dup (GSTM5)
ENST00000476321.5:n.708dup (GSTM3)
ENST00000486823.5:n.704dup (GSTM3)
ENST00000488824.1:n.1085dup (GSTM3)
NM_000849.4:c.*62dup (GSTM3) NP_000840.2:n.*62dup
NR_024537.1:n.974dup (GSTM3)
XM_011541296.1:c.*62dup (GSTM3) XP_011539598.1:n.*62dup
NM_000849.5:c.*62dup (GSTM3) MANE Select NP_000840.2:n.*62dup
NR_024537.2:n.974dup (GSTM3)