Canonical Allele Identifier: CA939081004

Gene: GSTP1

Linked Data

• dbSNP Id: rs1867452999
• gnomAD v3: 11-67585509-TCC-T
• gnomAD v4: 11-67585509-TCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67585510_67585511del , CM000673.2:g.67585510_67585511del	GRCh38
NC_000011.9:g.67352981_67352982del , CM000673.1:g.67352981_67352982del	GRCh37
NC_000011.8:g.67109557_67109558del	NCBI36
NG_012075.1:g.6916_6917del , LRG_723:g.6916_6917del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.336+269_336+270del	ENSP00000381604.1:n.336+269_336+270del
ENST00000398606.10:c.336+269_336+270del MANE Select	ENSP00000381607.3:n.336+269_336+270del
ENST00000646888.1:c.*52+269_*52+270del	ENSP00000494477.1:n.*52+269_*52+270del
ENST00000398603.5:c.336+269_336+270del	ENSP00000381604.1:n.336+269_336+270del
ENST00000398606.7:c.336+269_336+270del	ENSP00000381607.3:n.336+269_336+270del
ENST00000467591.1:n.447+269_447+270del
ENST00000494593.1:n.1131+269_1131+270del
ENST00000498765.5:c.399+269_399+270del
NM_000852.3:c.336+269_336+270del , LRG_723t1:c.336+269_336+270del	NP_000843.1:n.336+269_336+270del
NM_000852.4:c.336+269_336+270del MANE Select	NP_000843.1:n.336+269_336+270del