Canonical Allele Identifier: CA381521281
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586182G>A , CM000673.2:g.67586182G>A GRCh38
NC_000011.9:g.67353653G>A , CM000673.1:g.67353653G>A GRCh37
NC_000011.8:g.67110229G>A NCBI36
NG_012075.1:g.7588G>A , LRG_723:g.7588G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-207G>A ENSP00000381604.1:n.337-207G>A
ENST00000398606.10:c.415G>A MANE Select ENSP00000381607.3:p.Gly139Arg
ENST00000646888.1:c.*131G>A ENSP00000494477.1:n.*131G>A
ENST00000398603.5:c.337-207G>A ENSP00000381604.1:n.337-207G>A
ENST00000398606.7:c.415G>A ENSP00000381607.3:p.Gly139Arg
ENST00000467591.1:n.526G>A
ENST00000494593.1:n.1210G>A
ENST00000495996.1:c.79G>A ENSP00000484686.1:p.Gly27Arg
ENST00000498765.5:c.478G>A
NM_000852.3:c.415G>A , LRG_723t1:c.415G>A NP_000843.1:p.Gly139Arg
NM_000852.4:c.415G>A MANE Select NP_000843.1:p.Gly139Arg