Canonical Allele Identifier: CA381522919
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586483A>G , CM000673.2:g.67586483A>G GRCh38
NC_000011.9:g.67353954A>G , CM000673.1:g.67353954A>G GRCh37
NC_000011.8:g.67110530A>G NCBI36
NG_012075.1:g.7889A>G , LRG_723:g.7889A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.431A>G ENSP00000381604.1:p.Tyr144Cys
ENST00000398606.10:c.539A>G MANE Select ENSP00000381607.3:p.Tyr180Cys
ENST00000646888.1:c.*255A>G ENSP00000494477.1:n.*255A>G
ENST00000398603.5:c.431A>G ENSP00000381604.1:p.Tyr144Cys
ENST00000398606.7:c.539A>G ENSP00000381607.3:p.Tyr180Cys
ENST00000467591.1:n.650A>G
ENST00000494593.1:n.1511A>G
ENST00000498765.5:c.602A>G
NM_000852.3:c.539A>G , LRG_723t1:c.539A>G NP_000843.1:p.Tyr180Cys
NM_000852.4:c.539A>G MANE Select NP_000843.1:p.Tyr180Cys