Canonical Allele Identifier: CA381522310
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1867467385

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586399C>T , CM000673.2:g.67586399C>T GRCh38
NC_000011.9:g.67353870C>T , CM000673.1:g.67353870C>T GRCh37
NC_000011.8:g.67110446C>T NCBI36
NG_012075.1:g.7805C>T , LRG_723:g.7805C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.347C>T ENSP00000381604.1:p.Ala116Val
ENST00000398606.10:c.455C>T MANE Select ENSP00000381607.3:p.Ala152Val
ENST00000646888.1:c.*171C>T ENSP00000494477.1:n.*171C>T
ENST00000398603.5:c.347C>T ENSP00000381604.1:p.Ala116Val
ENST00000398606.7:c.455C>T ENSP00000381607.3:p.Ala152Val
ENST00000467591.1:n.566C>T
ENST00000494593.1:n.1427C>T
ENST00000495996.1:c.181C>T ENSP00000484686.1:p.Leu61=
ENST00000498765.5:c.518C>T
NM_000852.3:c.455C>T , LRG_723t1:c.455C>T NP_000843.1:p.Ala152Val
NM_000852.4:c.455C>T MANE Select NP_000843.1:p.Ala152Val