Canonical Allele Identifier: CA381522465
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586417A>T , CM000673.2:g.67586417A>T GRCh38
NC_000011.9:g.67353888A>T , CM000673.1:g.67353888A>T GRCh37
NC_000011.8:g.67110464A>T NCBI36
NG_012075.1:g.7823A>T , LRG_723:g.7823A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.365A>T ENSP00000381604.1:p.Asp122Val
ENST00000398606.10:c.473A>T MANE Select ENSP00000381607.3:p.Asp158Val
ENST00000646888.1:c.*189A>T ENSP00000494477.1:n.*189A>T
ENST00000398603.5:c.365A>T ENSP00000381604.1:p.Asp122Val
ENST00000398606.7:c.473A>T ENSP00000381607.3:p.Asp158Val
ENST00000467591.1:n.584A>T
ENST00000494593.1:n.1445A>T
ENST00000495996.1:c.199A>T ENSP00000484686.1:p.Thr67Ser
ENST00000498765.5:c.536A>T
NM_000852.3:c.473A>T , LRG_723t1:c.473A>T NP_000843.1:p.Asp158Val
NM_000852.4:c.473A>T MANE Select NP_000843.1:p.Asp158Val