Canonical Allele Identifier: CA341536017

Gene: GSTM3 GSTM5

Linked Data

• gnomAD v4: 1-109737389-A-C
• MyVariant Identifiers: chr1:g.110280011A>C (hg19) ; chr1:g.109737389A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737389A>C , CM000663.2:g.109737389A>C	GRCh38
NC_000001.10:g.110280011A>C , CM000663.1:g.110280011A>C	GRCh37
NC_000001.9:g.110081534A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.579+68T>G (GSTM3) MANE Select	ENSP00000354357.2:n.579+68T>G
ENST00000256594.7:c.579+68T>G (GSTM3)	ENSP00000256594.3:n.579+68T>G
ENST00000361066.6:c.579+68T>G (GSTM3)	ENSP00000354357.2:n.579+68T>G
ENST00000429410.2:n.82+25041A>C (GSTM5)
ENST00000476321.5:n.328T>G (GSTM3)
ENST00000486823.5:n.543+68T>G (GSTM3)
ENST00000488824.1:n.924+68T>G (GSTM3)
ENST00000540225.2:c.637T>G (GSTM3)	ENSP00000444978.2:p.Ter213Glu
NM_000849.4:c.579+68T>G (GSTM3)	NP_000840.2:n.579+68T>G
NR_024537.1:n.813+68T>G (GSTM3)
XM_011541296.1:c.798+68T>G (GSTM3)	XP_011539598.1:n.798+68T>G
NM_000849.5:c.579+68T>G (GSTM3) MANE Select	NP_000840.2:n.579+68T>G
NR_024537.2:n.813+68T>G (GSTM3)