Canonical Allele Identifier: CA525627020

Gene: GSTM3 GSTM5

Linked Data

• dbSNP Id: rs1393872933
• gnomAD v2: 1-110279771-GGCA-G
• gnomAD v3: 1-109737149-GGCA-G
• gnomAD v4: 1-109737149-GGCA-G
• MyVariant Identifiers: chr1:g.110279772_110279774del (hg19) ; chr1:g.109737150_109737152del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737152_109737154del , CM000663.2:g.109737152_109737154del	GRCh38
NC_000001.10:g.110279774_110279776del , CM000663.1:g.110279774_110279776del	GRCh37
NC_000001.9:g.110081297_110081299del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.597_599del (GSTM3) MANE Select	ENSP00000354357.2:p.Ala200del
ENST00000256594.7:c.597_599del (GSTM3)	ENSP00000256594.3:p.Ala200del
ENST00000361066.6:c.597_599del (GSTM3)	ENSP00000354357.2:p.Ala200del
ENST00000429410.2:n.82+24804_82+24806del (GSTM5)
ENST00000476321.5:n.565_567del (GSTM3)
ENST00000486823.5:n.561_563del (GSTM3)
ENST00000488824.1:n.942_944del (GSTM3)
NM_000849.4:c.597_599del (GSTM3)	NP_000840.2:p.Ala200del
NR_024537.1:n.831_833del (GSTM3)
XM_011541296.1:c.816_818del (GSTM3)	XP_011539598.1:p.Ala273del
NM_000849.5:c.597_599del (GSTM3) MANE Select	NP_000840.2:p.Ala200del
NR_024537.2:n.831_833del (GSTM3)