Canonical Allele Identifier: CA1980216035
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586195T= , CM000673.2:g.67586195T= GRCh38
NC_000011.9:g.67353666T= , CM000673.1:g.67353666T= GRCh37
NC_000011.8:g.67110242T= NCBI36
NG_012075.1:g.7601T= , LRG_723:g.7601T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-194T= ENSP00000381604.1:n.337-194T=
ENST00000398606.10:c.428T= MANE Select ENSP00000381607.3:p.Phe143=
ENST00000646888.1:c.*144T= ENSP00000494477.1:n.*144T=
ENST00000398603.5:c.337-194T= ENSP00000381604.1:n.337-194T=
ENST00000398606.7:c.428T= ENSP00000381607.3:p.Phe143=
ENST00000467591.1:n.539T=
ENST00000494593.1:n.1223T=
ENST00000495996.1:c.92T= ENSP00000484686.1:p.Phe31=
ENST00000498765.5:c.491T=
NM_000852.3:c.428T= , LRG_723t1:c.428T= NP_000843.1:p.Phe143=
NM_000852.4:c.428T= MANE Select NP_000843.1:p.Phe143=