Canonical Allele Identifier: CA381522956
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs752233998

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586491C>G , CM000673.2:g.67586491C>G GRCh38
NC_000011.9:g.67353962C>G , CM000673.1:g.67353962C>G GRCh37
NC_000011.8:g.67110538C>G NCBI36
NG_012075.1:g.7897C>G , LRG_723:g.7897C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.439C>G ENSP00000381604.1:p.Arg147Gly
ENST00000398606.10:c.547C>G MANE Select ENSP00000381607.3:p.Arg183Gly
ENST00000646888.1:c.*263C>G ENSP00000494477.1:n.*263C>G
ENST00000398603.5:c.439C>G ENSP00000381604.1:p.Arg147Gly
ENST00000398606.7:c.547C>G ENSP00000381607.3:p.Arg183Gly
ENST00000467591.1:n.658C>G
ENST00000494593.1:n.1519C>G
ENST00000498765.5:c.610C>G
NM_000852.3:c.547C>G , LRG_723t1:c.547C>G NP_000843.1:p.Arg183Gly
NM_000852.4:c.547C>G MANE Select NP_000843.1:p.Arg183Gly