Canonical Allele Identifier: CA419374447

Gene: GSTM3 GSTM5

Linked Data

• MyVariant Identifiers: chr1:g.110279711G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737089G>C , CM000663.2:g.109737089G>C	GRCh38
NC_000001.10:g.110279711G>C , CM000663.1:g.110279711G>C	GRCh37
NC_000001.9:g.110081234G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361066.7:c.660C>G (GSTM3) MANE Select	ENSP00000354357.2:p.Gly220=
ENST00000256594.7:c.660C>G (GSTM3)	ENSP00000256594.3:p.Gly220=
ENST00000361066.6:c.660C>G (GSTM3)	ENSP00000354357.2:p.Gly220=
ENST00000429410.2:n.82+24741G>C (GSTM5)
ENST00000476321.5:n.628C>G (GSTM3)
ENST00000486823.5:n.624C>G (GSTM3)
ENST00000488824.1:n.1005C>G (GSTM3)
NM_000849.4:c.660C>G (GSTM3)	NP_000840.2:p.Gly220=
NR_024537.1:n.894C>G (GSTM3)
XM_011541296.1:c.879C>G (GSTM3)	XP_011539598.1:p.Gly293=
NM_000849.5:c.660C>G (GSTM3) MANE Select	NP_000840.2:p.Gly220=
NR_024537.2:n.894C>G (GSTM3)