Canonical Allele Identifier: CA1980216282
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586403C= , CM000673.2:g.67586403C= GRCh38
NC_000011.9:g.67353874C= , CM000673.1:g.67353874C= GRCh37
NC_000011.8:g.67110450C= NCBI36
NG_012075.1:g.7809C= , LRG_723:g.7809C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.351C= ENSP00000381604.1:p.Asp117=
ENST00000398606.10:c.459C= MANE Select ENSP00000381607.3:p.Asp153=
ENST00000646888.1:c.*175C= ENSP00000494477.1:n.*175C=
ENST00000398603.5:c.351C= ENSP00000381604.1:p.Asp117=
ENST00000398606.7:c.459C= ENSP00000381607.3:p.Asp153=
ENST00000467591.1:n.570C=
ENST00000494593.1:n.1431C=
ENST00000495996.1:c.185C= ENSP00000484686.1:p.Thr62=
ENST00000498765.5:c.522C=
NM_000852.3:c.459C= , LRG_723t1:c.459C= NP_000843.1:p.Asp153=
NM_000852.4:c.459C= MANE Select NP_000843.1:p.Asp153=