Canonical Allele Identifier: CA419374468

Gene: GSTM3 GSTM5

Linked Data

• MyVariant Identifiers: chr1:g.110279732G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737110G>A , CM000663.2:g.109737110G>A	GRCh38
NC_000001.10:g.110279732G>A , CM000663.1:g.110279732G>A	GRCh37
NC_000001.9:g.110081255G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.639C>T (GSTM3) MANE Select	ENSP00000354357.2:p.Asn213=
ENST00000256594.7:c.639C>T (GSTM3)	ENSP00000256594.3:p.Asn213=
ENST00000361066.6:c.639C>T (GSTM3)	ENSP00000354357.2:p.Asn213=
ENST00000429410.2:n.82+24762G>A (GSTM5)
ENST00000476321.5:n.607C>T (GSTM3)
ENST00000486823.5:n.603C>T (GSTM3)
ENST00000488824.1:n.984C>T (GSTM3)
NM_000849.4:c.639C>T (GSTM3)	NP_000840.2:p.Asn213=
NR_024537.1:n.873C>T (GSTM3)
XM_011541296.1:c.858C>T (GSTM3)	XP_011539598.1:p.Asn286=
NM_000849.5:c.639C>T (GSTM3) MANE Select	NP_000840.2:p.Asn213=
NR_024537.2:n.873C>T (GSTM3)