Canonical Allele Identifier: CA381522329
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586401G>A , CM000673.2:g.67586401G>A GRCh38
NC_000011.9:g.67353872G>A , CM000673.1:g.67353872G>A GRCh37
NC_000011.8:g.67110448G>A NCBI36
NG_012075.1:g.7807G>A , LRG_723:g.7807G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.349G>A ENSP00000381604.1:p.Asp117Asn
ENST00000398606.10:c.457G>A MANE Select ENSP00000381607.3:p.Asp153Asn
ENST00000646888.1:c.*173G>A ENSP00000494477.1:n.*173G>A
ENST00000398603.5:c.349G>A ENSP00000381604.1:p.Asp117Asn
ENST00000398606.7:c.457G>A ENSP00000381607.3:p.Asp153Asn
ENST00000467591.1:n.568G>A
ENST00000494593.1:n.1429G>A
ENST00000495996.1:c.183G>A ENSP00000484686.1:p.Leu61=
ENST00000498765.5:c.520G>A
NM_000852.3:c.457G>A , LRG_723t1:c.457G>A NP_000843.1:p.Asp153Asn
NM_000852.4:c.457G>A MANE Select NP_000843.1:p.Asp153Asn