Canonical Allele Identifier: CA1980214958
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585320_67585321delinsTC , CM000673.2:g.67585320_67585321delinsTC GRCh38
NC_000011.9:g.67352791_67352792delinsTC , CM000673.1:g.67352791_67352792delinsTC GRCh37
NC_000011.8:g.67109367_67109368delinsTC NCBI36
NG_012075.1:g.6726_6727delinsTC , LRG_723:g.6726_6727delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.336+79_336+80delinsTC ENSP00000381604.1:n.336+79_336+80delinsTC
ENST00000398606.10:c.336+79_336+80delinsTC MANE Select ENSP00000381607.3:n.336+79_336+80delinsTC
ENST00000646888.1:c.*52+79_*52+80delinsTC ENSP00000494477.1:n.*52+79_*52+80delinsTC
ENST00000398603.5:c.336+79_336+80delinsTC ENSP00000381604.1:n.336+79_336+80delinsTC
ENST00000398606.7:c.336+79_336+80delinsTC ENSP00000381607.3:n.336+79_336+80delinsTC
ENST00000467591.1:n.447+79_447+80delinsTC
ENST00000494593.1:n.1131+79_1131+80delinsTC
ENST00000498765.5:c.399+79_399+80delinsTC
NM_000852.3:c.336+79_336+80delinsTC , LRG_723t1:c.336+79_336+80delinsTC NP_000843.1:n.336+79_336+80delinsTC
NM_000852.4:c.336+79_336+80delinsTC MANE Select NP_000843.1:n.336+79_336+80delinsTC