Canonical Allele Identifier: CA341535599

Gene: GSTM3 GSTM5

Linked Data

• gnomAD v4: 1-109737105-T-G
• MyVariant Identifiers: chr1:g.110279727T>G (hg19) ; chr1:g.109737105T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737105T>G , CM000663.2:g.109737105T>G	GRCh38
NC_000001.10:g.110279727T>G , CM000663.1:g.110279727T>G	GRCh37
NC_000001.9:g.110081250T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.644A>C (GSTM3) MANE Select	ENSP00000354357.2:p.Lys215Thr
ENST00000256594.7:c.644A>C (GSTM3)	ENSP00000256594.3:p.Lys215Thr
ENST00000361066.6:c.644A>C (GSTM3)	ENSP00000354357.2:p.Lys215Thr
ENST00000429410.2:n.82+24757T>G (GSTM5)
ENST00000476321.5:n.612A>C (GSTM3)
ENST00000486823.5:n.608A>C (GSTM3)
ENST00000488824.1:n.989A>C (GSTM3)
NM_000849.4:c.644A>C (GSTM3)	NP_000840.2:p.Lys215Thr
NR_024537.1:n.878A>C (GSTM3)
XM_011541296.1:c.863A>C (GSTM3)	XP_011539598.1:p.Lys288Thr
NM_000849.5:c.644A>C (GSTM3) MANE Select	NP_000840.2:p.Lys215Thr
NR_024537.2:n.878A>C (GSTM3)