Canonical Allele Identifier: CA1980215236
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585656_67585666delinsAGCGTGTGTGC , CM000673.2:g.67585656_67585666delinsAGCGTGTGTGC GRCh38
NC_000011.9:g.67353127_67353137delinsAGCGTGTGTGC , CM000673.1:g.67353127_67353137delinsAGCGTGTGTGC GRCh37
NC_000011.8:g.67109703_67109713delinsAGCGTGTGTGC NCBI36
NG_012075.1:g.7062_7072delinsAGCGTGTGTGC , LRG_723:g.7062_7072delinsAGCGTGTGTGC

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.336+415_336+425delinsAGCGTGTGTGC ENSP00000381604.1:n.336+415_336+425delinsAGCGTGTGTGC
ENST00000398606.10:c.336+415_336+425delinsAGCGTGTGTGC MANE Select ENSP00000381607.3:n.336+415_336+425delinsAGCGTGTGTGC
ENST00000646888.1:c.*52+415_*52+425delinsAGCGTGTGTGC ENSP00000494477.1:n.*52+415_*52+425delinsAGCGTGTGTGC
ENST00000398603.5:c.336+415_336+425delinsAGCGTGTGTGC ENSP00000381604.1:n.336+415_336+425delinsAGCGTGTGTGC
ENST00000398606.7:c.336+415_336+425delinsAGCGTGTGTGC ENSP00000381607.3:n.336+415_336+425delinsAGCGTGTGTGC
ENST00000467591.1:n.447+415_447+425delinsAGCGTGTGTGC
ENST00000494593.1:n.1131+415_1131+425delinsAGCGTGTGTGC
ENST00000498765.5:c.399+415_399+425delinsAGCGTGTGTGC
NM_000852.3:c.336+415_336+425delinsAGCGTGTGTGC , LRG_723t1:c.336+415_336+425delinsAGCGTGTGTGC NP_000843.1:n.336+415_336+425delinsAGCGTGTGTGC
NM_000852.4:c.336+415_336+425delinsAGCGTGTGTGC MANE Select NP_000843.1:n.336+415_336+425delinsAGCGTGTGTGC