Canonical Allele Identifier: CA1980215222
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585635T= , CM000673.2:g.67585635T= GRCh38
NC_000011.9:g.67353106T= , CM000673.1:g.67353106T= GRCh37
NC_000011.8:g.67109682T= NCBI36
NG_012075.1:g.7041T= , LRG_723:g.7041T=

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.336+394T= ENSP00000381604.1:n.336+394T=
ENST00000398606.10:c.336+394T= MANE Select ENSP00000381607.3:n.336+394T=
ENST00000646888.1:c.*52+394T= ENSP00000494477.1:n.*52+394T=
ENST00000398603.5:c.336+394T= ENSP00000381604.1:n.336+394T=
ENST00000398606.7:c.336+394T= ENSP00000381607.3:n.336+394T=
ENST00000467591.1:n.447+394T=
ENST00000494593.1:n.1131+394T=
ENST00000498765.5:c.399+394T=
NM_000852.3:c.336+394T= , LRG_723t1:c.336+394T= NP_000843.1:n.336+394T=
NM_000852.4:c.336+394T= MANE Select NP_000843.1:n.336+394T=