Canonical Allele Identifier: CA381522648
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1591100810

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586437G>A , CM000673.2:g.67586437G>A GRCh38
NC_000011.9:g.67353908G>A , CM000673.1:g.67353908G>A GRCh37
NC_000011.8:g.67110484G>A NCBI36
NG_012075.1:g.7843G>A , LRG_723:g.7843G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.385G>A ENSP00000381604.1:p.Val129Ile
ENST00000398606.10:c.493G>A MANE Select ENSP00000381607.3:p.Val165Ile
ENST00000646888.1:c.*209G>A ENSP00000494477.1:n.*209G>A
ENST00000398603.5:c.385G>A ENSP00000381604.1:p.Val129Ile
ENST00000398606.7:c.493G>A ENSP00000381607.3:p.Val165Ile
ENST00000467591.1:n.604G>A
ENST00000494593.1:n.1465G>A
ENST00000495996.1:c.219G>A ENSP00000484686.1:n.219G>A
ENST00000498765.5:c.556G>A
NM_000852.3:c.493G>A , LRG_723t1:c.493G>A NP_000843.1:p.Val165Ile
NM_000852.4:c.493G>A MANE Select NP_000843.1:p.Val165Ile