Canonical Allele Identifier: CA1980214890

Gene: GSTP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67585269_67585270delinsTG , CM000673.2:g.67585269_67585270delinsTG	GRCh38
NC_000011.9:g.67352740_67352741delinsTG , CM000673.1:g.67352740_67352741delinsTG	GRCh37
NC_000011.8:g.67109316_67109317delinsTG	NCBI36
NG_012075.1:g.6675_6676delinsTG , LRG_723:g.6675_6676delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.336+28_336+29delinsTG	ENSP00000381604.1:n.336+28_336+29delinsTG
ENST00000398606.10:c.336+28_336+29delinsTG MANE Select	ENSP00000381607.3:n.336+28_336+29delinsTG
ENST00000646888.1:c.*52+28_*52+29delinsTG	ENSP00000494477.1:n.*52+28_*52+29delinsTG
ENST00000398603.5:c.336+28_336+29delinsTG	ENSP00000381604.1:n.336+28_336+29delinsTG
ENST00000398606.7:c.336+28_336+29delinsTG	ENSP00000381607.3:n.336+28_336+29delinsTG
ENST00000467591.1:n.447+28_447+29delinsTG
ENST00000494593.1:n.1131+28_1131+29delinsTG
ENST00000498765.5:c.399+28_399+29delinsTG
NM_000852.3:c.336+28_336+29delinsTG , LRG_723t1:c.336+28_336+29delinsTG	NP_000843.1:n.336+28_336+29delinsTG
NM_000852.4:c.336+28_336+29delinsTG MANE Select	NP_000843.1:n.336+28_336+29delinsTG