Canonical Allele Identifier: CA2614645988
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585198_67585199insTTTTTTTAAT , CM000673.2:g.67585198_67585199insTTTTTTTAAT GRCh38
NC_000011.9:g.67352669_67352670insTTTTTTTAAT , CM000673.1:g.67352669_67352670insTTTTTTTAAT GRCh37
NC_000011.8:g.67109245_67109246insTTTTTTTAAT NCBI36
NG_012075.1:g.6604_6605insTTTTTTTAAT , LRG_723:g.6604_6605insTTTTTTTAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.293_294insTTTTTTTAAT ENSP00000381604.1:p.Glu98AspfsTer23
ENST00000398606.10:c.293_294insTTTTTTTAAT MANE Select ENSP00000381607.3:p.Glu98AspfsTer19
ENST00000646888.1:c.*9_*10insTTTTTTTAAT ENSP00000494477.1:n.*9_*10insTTTTTTTAAT
ENST00000398603.5:c.293_294insTTTTTTTAAT ENSP00000381604.1:p.Glu98AspfsTer23
ENST00000398606.7:c.293_294insTTTTTTTAAT ENSP00000381607.3:p.Glu98AspfsTer19
ENST00000467591.1:n.404_405insTTTTTTTAAT
ENST00000494593.1:n.1088_1089insTTTTTTTAAT
ENST00000498765.5:c.356_357insTTTTTTTAAT
NM_000852.3:c.293_294insTTTTTTTAAT , LRG_723t1:c.293_294insTTTTTTTAAT NP_000843.1:p.Glu98AspfsTer19
NM_000852.4:c.293_294insTTTTTTTAAT MANE Select NP_000843.1:p.Glu98AspfsTer19