Canonical Allele Identifier: CA381519895
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585231A>G , CM000673.2:g.67585231A>G GRCh38
NC_000011.9:g.67352702A>G , CM000673.1:g.67352702A>G GRCh37
NC_000011.8:g.67109278A>G NCBI36
NG_012075.1:g.6637A>G , LRG_723:g.6637A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.326A>G ENSP00000381604.1:p.Tyr109Cys
ENST00000398606.10:c.326A>G MANE Select ENSP00000381607.3:p.Tyr109Cys
ENST00000646888.1:c.*42A>G ENSP00000494477.1:n.*42A>G
ENST00000398603.5:c.326A>G ENSP00000381604.1:p.Tyr109Cys
ENST00000398606.7:c.326A>G ENSP00000381607.3:p.Tyr109Cys
ENST00000467591.1:n.437A>G
ENST00000494593.1:n.1121A>G
ENST00000498765.5:c.389A>G
NM_000852.3:c.326A>G , LRG_723t1:c.326A>G NP_000843.1:p.Tyr109Cys
NM_000852.4:c.326A>G MANE Select NP_000843.1:p.Tyr109Cys