Canonical Allele Identifier: CA341536046

Gene: GSTM3 GSTM5

Linked Data

• gnomAD v4: 1-109737392-G-A
• MyVariant Identifiers: chr1:g.110280014G>A (hg19) ; chr1:g.109737392G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737392G>A , CM000663.2:g.109737392G>A	GRCh38
NC_000001.10:g.110280014G>A , CM000663.1:g.110280014G>A	GRCh37
NC_000001.9:g.110081537G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.579+65C>T (GSTM3) MANE Select	ENSP00000354357.2:n.579+65C>T
ENST00000256594.7:c.579+65C>T (GSTM3)	ENSP00000256594.3:n.579+65C>T
ENST00000361066.6:c.579+65C>T (GSTM3)	ENSP00000354357.2:n.579+65C>T
ENST00000429410.2:n.82+25044G>A (GSTM5)
ENST00000476321.5:n.325C>T (GSTM3)
ENST00000486823.5:n.543+65C>T (GSTM3)
ENST00000488824.1:n.924+65C>T (GSTM3)
ENST00000540225.2:c.634C>T (GSTM3)	ENSP00000444978.2:p.Pro212Ser
NM_000849.4:c.579+65C>T (GSTM3)	NP_000840.2:n.579+65C>T
NR_024537.1:n.813+65C>T (GSTM3)
XM_011541296.1:c.798+65C>T (GSTM3)	XP_011539598.1:n.798+65C>T
NM_000849.5:c.579+65C>T (GSTM3) MANE Select	NP_000840.2:n.579+65C>T
NR_024537.2:n.813+65C>T (GSTM3)