Canonical Allele Identifier: CA1980216297
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586410C= , CM000673.2:g.67586410C= GRCh38
NC_000011.9:g.67353881C= , CM000673.1:g.67353881C= GRCh37
NC_000011.8:g.67110457C= NCBI36
NG_012075.1:g.7816C= , LRG_723:g.7816C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.358C= ENSP00000381604.1:p.Leu120=
ENST00000398606.10:c.466C= MANE Select ENSP00000381607.3:p.Leu156=
ENST00000646888.1:c.*182C= ENSP00000494477.1:n.*182C=
ENST00000398603.5:c.358C= ENSP00000381604.1:p.Leu120=
ENST00000398606.7:c.466C= ENSP00000381607.3:p.Leu156=
ENST00000467591.1:n.577C=
ENST00000494593.1:n.1438C=
ENST00000495996.1:c.192C= ENSP00000484686.1:p.Thr64=
ENST00000498765.5:c.529C=
NM_000852.3:c.466C= , LRG_723t1:c.466C= NP_000843.1:p.Leu156=
NM_000852.4:c.466C= MANE Select NP_000843.1:p.Leu156=