Canonical Allele Identifier: CA1980215227
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585645_67585648delinsTCAG , CM000673.2:g.67585645_67585648delinsTCAG GRCh38
NC_000011.9:g.67353116_67353119delinsTCAG , CM000673.1:g.67353116_67353119delinsTCAG GRCh37
NC_000011.8:g.67109692_67109695delinsTCAG NCBI36
NG_012075.1:g.7051_7054delinsTCAG , LRG_723:g.7051_7054delinsTCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.336+404_336+407delinsTCAG ENSP00000381604.1:n.336+404_336+407delinsTCAG
ENST00000398606.10:c.336+404_336+407delinsTCAG MANE Select ENSP00000381607.3:n.336+404_336+407delinsTCAG
ENST00000646888.1:c.*52+404_*52+407delinsTCAG ENSP00000494477.1:n.*52+404_*52+407delinsTCAG
ENST00000398603.5:c.336+404_336+407delinsTCAG ENSP00000381604.1:n.336+404_336+407delinsTCAG
ENST00000398606.7:c.336+404_336+407delinsTCAG ENSP00000381607.3:n.336+404_336+407delinsTCAG
ENST00000467591.1:n.447+404_447+407delinsTCAG
ENST00000494593.1:n.1131+404_1131+407delinsTCAG
ENST00000498765.5:c.399+404_399+407delinsTCAG
NM_000852.3:c.336+404_336+407delinsTCAG , LRG_723t1:c.336+404_336+407delinsTCAG NP_000843.1:n.336+404_336+407delinsTCAG
NM_000852.4:c.336+404_336+407delinsTCAG MANE Select NP_000843.1:n.336+404_336+407delinsTCAG