Canonical Allele Identifier: CA1980216058
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586206G= , CM000673.2:g.67586206G= GRCh38
NC_000011.9:g.67353677G= , CM000673.1:g.67353677G= GRCh37
NC_000011.8:g.67110253G= NCBI36
NG_012075.1:g.7612G= , LRG_723:g.7612G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-183G= ENSP00000381604.1:n.337-183G=
ENST00000398606.10:c.439G= MANE Select ENSP00000381607.3:p.Asp147=
ENST00000646888.1:c.*155G= ENSP00000494477.1:n.*155G=
ENST00000398603.5:c.337-183G= ENSP00000381604.1:n.337-183G=
ENST00000398606.7:c.439G= ENSP00000381607.3:p.Asp147=
ENST00000467591.1:n.550G=
ENST00000494593.1:n.1234G=
ENST00000495996.1:c.103G= ENSP00000484686.1:p.Asp35=
ENST00000498765.5:c.502G=
NM_000852.3:c.439G= , LRG_723t1:c.439G= NP_000843.1:p.Asp147=
NM_000852.4:c.439G= MANE Select NP_000843.1:p.Asp147=