Canonical Allele Identifier: CA1980213922
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584706T= , CM000673.2:g.67584706T= GRCh38
NC_000011.9:g.67352177T= , CM000673.1:g.67352177T= GRCh37
NC_000011.8:g.67108753T= NCBI36
NG_012075.1:g.6112T= , LRG_723:g.6112T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.166T= ENSP00000381604.1:p.Phe56=
ENST00000398606.10:c.166T= MANE Select ENSP00000381607.3:p.Phe56=
ENST00000646888.1:c.59T= ENSP00000494477.1:p.Val20=
ENST00000398603.5:c.166T= ENSP00000381604.1:p.Phe56=
ENST00000398606.7:c.166T= ENSP00000381607.3:p.Phe56=
ENST00000489040.1:n.165T=
ENST00000494593.1:n.596T=
ENST00000498765.5:c.129T=
NM_000852.3:c.166T= , LRG_723t1:c.166T= NP_000843.1:p.Phe56=
NM_000852.4:c.166T= MANE Select NP_000843.1:p.Phe56=