Canonical Allele Identifier: CA381522235
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586391C>G , CM000673.2:g.67586391C>G GRCh38
NC_000011.9:g.67353862C>G , CM000673.1:g.67353862C>G GRCh37
NC_000011.8:g.67110438C>G NCBI36
NG_012075.1:g.7797C>G , LRG_723:g.7797C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.339C>G ENSP00000381604.1:p.Ile113Met
ENST00000398606.10:c.447C>G MANE Select ENSP00000381607.3:p.Ile149Met
ENST00000646888.1:c.*163C>G ENSP00000494477.1:n.*163C>G
ENST00000398603.5:c.339C>G ENSP00000381604.1:p.Ile113Met
ENST00000398606.7:c.447C>G ENSP00000381607.3:p.Ile149Met
ENST00000467591.1:n.558C>G
ENST00000494593.1:n.1419C>G
ENST00000495996.1:c.173C>G ENSP00000484686.1:p.Ser58Cys
ENST00000498765.5:c.510C>G
NM_000852.3:c.447C>G , LRG_723t1:c.447C>G NP_000843.1:p.Ile149Met
NM_000852.4:c.447C>G MANE Select NP_000843.1:p.Ile149Met