Canonical Allele Identifier: CA381522035
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586258C>A , CM000673.2:g.67586258C>A GRCh38
NC_000011.9:g.67353729C>A , CM000673.1:g.67353729C>A GRCh37
NC_000011.8:g.67110305C>A NCBI36
NG_012075.1:g.7664C>A , LRG_723:g.7664C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-131C>A ENSP00000381604.1:n.337-131C>A
ENST00000398606.10:c.444+47C>A MANE Select ENSP00000381607.3:n.444+47C>A
ENST00000646888.1:c.*160+47C>A ENSP00000494477.1:n.*160+47C>A
ENST00000398603.5:c.337-131C>A ENSP00000381604.1:n.337-131C>A
ENST00000398606.7:c.444+47C>A ENSP00000381607.3:n.444+47C>A
ENST00000467591.1:n.555+47C>A
ENST00000494593.1:n.1286C>A
ENST00000495996.1:c.155C>A ENSP00000484686.1:p.Ser52Tyr
ENST00000498765.5:c.507+47C>A
NM_000852.3:c.444+47C>A , LRG_723t1:c.444+47C>A NP_000843.1:n.444+47C>A
NM_000852.4:c.444+47C>A MANE Select NP_000843.1:n.444+47C>A