Canonical Allele Identifier: CA2614645338
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584892G>A , CM000673.2:g.67584892G>A GRCh38
NC_000011.9:g.67352363G>A , CM000673.1:g.67352363G>A GRCh37
NC_000011.8:g.67108939G>A NCBI36
NG_012075.1:g.6298G>A , LRG_723:g.6298G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.232+120G>A ENSP00000381604.1:n.232+120G>A
ENST00000398606.10:c.232+120G>A MANE Select ENSP00000381607.3:n.232+120G>A
ENST00000646888.1:c.125+120G>A ENSP00000494477.1:n.125+120G>A
ENST00000398603.5:c.232+120G>A ENSP00000381604.1:n.232+120G>A
ENST00000398606.7:c.232+120G>A ENSP00000381607.3:n.232+120G>A
ENST00000467591.1:n.98G>A
ENST00000489040.1:n.351G>A
ENST00000494593.1:n.782G>A
ENST00000498765.5:c.195+120G>A
NM_000852.3:c.232+120G>A , LRG_723t1:c.232+120G>A NP_000843.1:n.232+120G>A
NM_000852.4:c.232+120G>A MANE Select NP_000843.1:n.232+120G>A