Canonical Allele Identifier: CA419374458

Gene: GSTM3 GSTM5

Linked Data

• MyVariant Identifiers: chr1:g.110279720G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737098G>C , CM000663.2:g.109737098G>C	GRCh38
NC_000001.10:g.110279720G>C , CM000663.1:g.110279720G>C	GRCh37
NC_000001.9:g.110081243G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.651C>G (GSTM3) MANE Select	ENSP00000354357.2:p.Ala217=
ENST00000256594.7:c.651C>G (GSTM3)	ENSP00000256594.3:p.Ala217=
ENST00000361066.6:c.651C>G (GSTM3)	ENSP00000354357.2:p.Ala217=
ENST00000429410.2:n.82+24750G>C (GSTM5)
ENST00000476321.5:n.619C>G (GSTM3)
ENST00000486823.5:n.615C>G (GSTM3)
ENST00000488824.1:n.996C>G (GSTM3)
NM_000849.4:c.651C>G (GSTM3)	NP_000840.2:p.Ala217=
NR_024537.1:n.885C>G (GSTM3)
XM_011541296.1:c.870C>G (GSTM3)	XP_011539598.1:p.Ala290=
NM_000849.5:c.651C>G (GSTM3) MANE Select	NP_000840.2:p.Ala217=
NR_024537.2:n.885C>G (GSTM3)