Canonical Allele Identifier: CA381519964
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs770460061

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585239T>A , CM000673.2:g.67585239T>A GRCh38
NC_000011.9:g.67352710T>A , CM000673.1:g.67352710T>A GRCh37
NC_000011.8:g.67109286T>A NCBI36
NG_012075.1:g.6645T>A , LRG_723:g.6645T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.334T>A ENSP00000381604.1:p.Tyr112Asn
ENST00000398606.10:c.334T>A MANE Select ENSP00000381607.3:p.Tyr112Asn
ENST00000646888.1:c.*50T>A ENSP00000494477.1:n.*50T>A
ENST00000398603.5:c.334T>A ENSP00000381604.1:p.Tyr112Asn
ENST00000398606.7:c.334T>A ENSP00000381607.3:p.Tyr112Asn
ENST00000467591.1:n.445T>A
ENST00000494593.1:n.1129T>A
ENST00000498765.5:c.397T>A
NM_000852.3:c.334T>A , LRG_723t1:c.334T>A NP_000843.1:p.Tyr112Asn
NM_000852.4:c.334T>A MANE Select NP_000843.1:p.Tyr112Asn