Canonical Allele Identifier: CA1980215982
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586166G= , CM000673.2:g.67586166G= GRCh38
NC_000011.9:g.67353637G= , CM000673.1:g.67353637G= GRCh37
NC_000011.8:g.67110213G= NCBI36
NG_012075.1:g.7572G= , LRG_723:g.7572G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-223G= ENSP00000381604.1:n.337-223G=
ENST00000398606.10:c.399G= MANE Select ENSP00000381607.3:p.Leu133=
ENST00000646888.1:c.*115G= ENSP00000494477.1:n.*115G=
ENST00000398603.5:c.337-223G= ENSP00000381604.1:n.337-223G=
ENST00000398606.7:c.399G= ENSP00000381607.3:p.Leu133=
ENST00000467591.1:n.510G=
ENST00000494593.1:n.1194G=
ENST00000495996.1:c.63G= ENSP00000484686.1:p.Leu21=
ENST00000498765.5:c.462G=
NM_000852.3:c.399G= , LRG_723t1:c.399G= NP_000843.1:p.Leu133=
NM_000852.4:c.399G= MANE Select NP_000843.1:p.Leu133=