Canonical Allele Identifier: CA381519122
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs990829761

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585188G>A , CM000673.2:g.67585188G>A GRCh38
NC_000011.9:g.67352659G>A , CM000673.1:g.67352659G>A GRCh37
NC_000011.8:g.67109235G>A NCBI36
NG_012075.1:g.6594G>A , LRG_723:g.6594G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.283G>A ENSP00000381604.1:p.Asp95Asn
ENST00000398606.10:c.283G>A MANE Select ENSP00000381607.3:p.Asp95Asn
ENST00000646888.1:c.176G>A ENSP00000494477.1:p.Ter59=
ENST00000398603.5:c.283G>A ENSP00000381604.1:p.Asp95Asn
ENST00000398606.7:c.283G>A ENSP00000381607.3:p.Asp95Asn
ENST00000467591.1:n.394G>A
ENST00000494593.1:n.1078G>A
ENST00000498765.5:c.346G>A
NM_000852.3:c.283G>A , LRG_723t1:c.283G>A NP_000843.1:p.Asp95Asn
NM_000852.4:c.283G>A MANE Select NP_000843.1:p.Asp95Asn