Canonical Allele Identifier: CA6142887
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs770923997

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586460T>G , CM000673.2:g.67586460T>G GRCh38
NC_000011.9:g.67353931T>G , CM000673.1:g.67353931T>G GRCh37
NC_000011.8:g.67110507T>G NCBI36
NG_012075.1:g.7866T>G , LRG_723:g.7866T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.408T>G ENSP00000381604.1:p.Asp136Glu
ENST00000398606.10:c.516T>G MANE Select ENSP00000381607.3:p.Asp172Glu
ENST00000646888.1:c.*232T>G ENSP00000494477.1:n.*232T>G
ENST00000398603.5:c.408T>G ENSP00000381604.1:p.Asp136Glu
ENST00000398606.7:c.516T>G ENSP00000381607.3:p.Asp172Glu
ENST00000467591.1:n.627T>G
ENST00000494593.1:n.1488T>G
ENST00000498765.5:c.579T>G
NM_000852.3:c.516T>G , LRG_723t1:c.516T>G NP_000843.1:p.Asp172Glu
NM_000852.4:c.516T>G MANE Select NP_000843.1:p.Asp172Glu