Canonical Allele Identifier: CA1980215903
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586118T= , CM000673.2:g.67586118T= GRCh38
NC_000011.9:g.67353589T= , CM000673.1:g.67353589T= GRCh37
NC_000011.8:g.67110165T= NCBI36
NG_012075.1:g.7524T= , LRG_723:g.7524T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-271T= ENSP00000381604.1:n.337-271T=
ENST00000398606.10:c.351T= MANE Select ENSP00000381607.3:p.Asp117=
ENST00000646888.1:c.*67T= ENSP00000494477.1:n.*67T=
ENST00000398603.5:c.337-271T= ENSP00000381604.1:n.337-271T=
ENST00000398606.7:c.351T= ENSP00000381607.3:p.Asp117=
ENST00000467591.1:n.462T=
ENST00000494593.1:n.1146T=
ENST00000495996.1:c.15T= ENSP00000484686.1:p.Asp5=
ENST00000498765.5:c.414T=
NM_000852.3:c.351T= , LRG_723t1:c.351T= NP_000843.1:p.Asp117=
NM_000852.4:c.351T= MANE Select NP_000843.1:p.Asp117=