Canonical Allele Identifier: CA2614645488
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584951T>A , CM000673.2:g.67584951T>A GRCh38
NC_000011.9:g.67352422T>A , CM000673.1:g.67352422T>A GRCh37
NC_000011.8:g.67108998T>A NCBI36
NG_012075.1:g.6357T>A , LRG_723:g.6357T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.232+179T>A ENSP00000381604.1:n.232+179T>A
ENST00000398606.10:c.232+179T>A MANE Select ENSP00000381607.3:n.232+179T>A
ENST00000646888.1:c.125+179T>A ENSP00000494477.1:n.125+179T>A
ENST00000398603.5:c.232+179T>A ENSP00000381604.1:n.232+179T>A
ENST00000398606.7:c.232+179T>A ENSP00000381607.3:n.232+179T>A
ENST00000467591.1:n.157T>A
ENST00000489040.1:n.410T>A
ENST00000494593.1:n.841T>A
ENST00000498765.5:c.196-87T>A
NM_000852.3:c.232+179T>A , LRG_723t1:c.232+179T>A NP_000843.1:n.232+179T>A
NM_000852.4:c.232+179T>A MANE Select NP_000843.1:n.232+179T>A