Canonical Allele Identifier: CA525627042

Gene: GSTM3 GSTM5

Linked Data

• dbSNP Id: rs1292746371
• gnomAD v2: 1-110280001-ATCC-A
• gnomAD v4: 1-109737379-ATCC-A
• MyVariant Identifiers: chr1:g.110280002_110280004del (hg19) ; chr1:g.109737380_109737382del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737383_109737385del , CM000663.2:g.109737383_109737385del	GRCh38
NC_000001.10:g.110280005_110280007del , CM000663.1:g.110280005_110280007del	GRCh37
NC_000001.9:g.110081528_110081530del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.579+75_579+77del (GSTM3) MANE Select	ENSP00000354357.2:n.579+75_579+77del
ENST00000256594.7:c.579+75_579+77del (GSTM3)	ENSP00000256594.3:n.579+75_579+77del
ENST00000361066.6:c.579+75_579+77del (GSTM3)	ENSP00000354357.2:n.579+75_579+77del
ENST00000429410.2:n.82+25035_82+25037del (GSTM5)
ENST00000476321.5:n.335_337del (GSTM3)
ENST00000486823.5:n.543+75_543+77del (GSTM3)
ENST00000488824.1:n.924+75_924+77del (GSTM3)
ENST00000540225.2:c.*5_*7del (GSTM3)	ENSP00000444978.2:n.*5_*7del
NM_000849.4:c.579+75_579+77del (GSTM3)	NP_000840.2:n.579+75_579+77del
NR_024537.1:n.813+75_813+77del (GSTM3)
XM_011541296.1:c.798+75_798+77del (GSTM3)	XP_011539598.1:n.798+75_798+77del
NM_000849.5:c.579+75_579+77del (GSTM3) MANE Select	NP_000840.2:n.579+75_579+77del
NR_024537.2:n.813+75_813+77del (GSTM3)