Canonical Allele Identifier: CA1980216029
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586192C= , CM000673.2:g.67586192C= GRCh38
NC_000011.9:g.67353663C= , CM000673.1:g.67353663C= GRCh37
NC_000011.8:g.67110239C= NCBI36
NG_012075.1:g.7598C= , LRG_723:g.7598C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-197C= ENSP00000381604.1:n.337-197C=
ENST00000398606.10:c.425C= MANE Select ENSP00000381607.3:p.Thr142=
ENST00000646888.1:c.*141C= ENSP00000494477.1:n.*141C=
ENST00000398603.5:c.337-197C= ENSP00000381604.1:n.337-197C=
ENST00000398606.7:c.425C= ENSP00000381607.3:p.Thr142=
ENST00000467591.1:n.536C=
ENST00000494593.1:n.1220C=
ENST00000495996.1:c.89C= ENSP00000484686.1:p.Thr30=
ENST00000498765.5:c.488C=
NM_000852.3:c.425C= , LRG_723t1:c.425C= NP_000843.1:p.Thr142=
NM_000852.4:c.425C= MANE Select NP_000843.1:p.Thr142=