Canonical Allele Identifier: CA1980215138
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585509_67585511delinsTCC , CM000673.2:g.67585509_67585511delinsTCC GRCh38
NC_000011.9:g.67352980_67352982delinsTCC , CM000673.1:g.67352980_67352982delinsTCC GRCh37
NC_000011.8:g.67109556_67109558delinsTCC NCBI36
NG_012075.1:g.6915_6917delinsTCC , LRG_723:g.6915_6917delinsTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.336+268_336+270delinsTCC ENSP00000381604.1:n.336+268_336+270delinsTCC
ENST00000398606.10:c.336+268_336+270delinsTCC MANE Select ENSP00000381607.3:n.336+268_336+270delinsTCC
ENST00000646888.1:c.*52+268_*52+270delinsTCC ENSP00000494477.1:n.*52+268_*52+270delinsTCC
ENST00000398603.5:c.336+268_336+270delinsTCC ENSP00000381604.1:n.336+268_336+270delinsTCC
ENST00000398606.7:c.336+268_336+270delinsTCC ENSP00000381607.3:n.336+268_336+270delinsTCC
ENST00000467591.1:n.447+268_447+270delinsTCC
ENST00000494593.1:n.1131+268_1131+270delinsTCC
ENST00000498765.5:c.399+268_399+270delinsTCC
NM_000852.3:c.336+268_336+270delinsTCC , LRG_723t1:c.336+268_336+270delinsTCC NP_000843.1:n.336+268_336+270delinsTCC
NM_000852.4:c.336+268_336+270delinsTCC MANE Select NP_000843.1:n.336+268_336+270delinsTCC