Canonical Allele Identifier: CA381521142
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586171C>G , CM000673.2:g.67586171C>G GRCh38
NC_000011.9:g.67353642C>G , CM000673.1:g.67353642C>G GRCh37
NC_000011.8:g.67110218C>G NCBI36
NG_012075.1:g.7577C>G , LRG_723:g.7577C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-218C>G ENSP00000381604.1:n.337-218C>G
ENST00000398606.10:c.404C>G MANE Select ENSP00000381607.3:p.Ser135Cys
ENST00000646888.1:c.*120C>G ENSP00000494477.1:n.*120C>G
ENST00000398603.5:c.337-218C>G ENSP00000381604.1:n.337-218C>G
ENST00000398606.7:c.404C>G ENSP00000381607.3:p.Ser135Cys
ENST00000467591.1:n.515C>G
ENST00000494593.1:n.1199C>G
ENST00000495996.1:c.68C>G ENSP00000484686.1:p.Ser23Cys
ENST00000498765.5:c.467C>G
NM_000852.3:c.404C>G , LRG_723t1:c.404C>G NP_000843.1:p.Ser135Cys
NM_000852.4:c.404C>G MANE Select NP_000843.1:p.Ser135Cys