Canonical Allele Identifier: CA1980216013
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586183G= , CM000673.2:g.67586183G= GRCh38
NC_000011.9:g.67353654G= , CM000673.1:g.67353654G= GRCh37
NC_000011.8:g.67110230G= NCBI36
NG_012075.1:g.7589G= , LRG_723:g.7589G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-206G= ENSP00000381604.1:n.337-206G=
ENST00000398606.10:c.416G= MANE Select ENSP00000381607.3:p.Gly139=
ENST00000646888.1:c.*132G= ENSP00000494477.1:n.*132G=
ENST00000398603.5:c.337-206G= ENSP00000381604.1:n.337-206G=
ENST00000398606.7:c.416G= ENSP00000381607.3:p.Gly139=
ENST00000467591.1:n.527G=
ENST00000494593.1:n.1211G=
ENST00000495996.1:c.80G= ENSP00000484686.1:p.Gly27=
ENST00000498765.5:c.479G=
NM_000852.3:c.416G= , LRG_723t1:c.416G= NP_000843.1:p.Gly139=
NM_000852.4:c.416G= MANE Select NP_000843.1:p.Gly139=