Canonical Allele Identifier: CA1980216349
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586434G= , CM000673.2:g.67586434G= GRCh38
NC_000011.9:g.67353905G= , CM000673.1:g.67353905G= GRCh37
NC_000011.8:g.67110481G= NCBI36
NG_012075.1:g.7840G= , LRG_723:g.7840G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.382G= ENSP00000381604.1:p.Glu128=
ENST00000398606.10:c.490G= MANE Select ENSP00000381607.3:p.Glu164=
ENST00000646888.1:c.*206G= ENSP00000494477.1:n.*206G=
ENST00000398603.5:c.382G= ENSP00000381604.1:p.Glu128=
ENST00000398606.7:c.490G= ENSP00000381607.3:p.Glu164=
ENST00000467591.1:n.601G=
ENST00000494593.1:n.1462G=
ENST00000495996.1:c.216G= ENSP00000484686.1:n.216G=
ENST00000498765.5:c.553G=
NM_000852.3:c.490G= , LRG_723t1:c.490G= NP_000843.1:p.Glu164=
NM_000852.4:c.490G= MANE Select NP_000843.1:p.Glu164=