Canonical Allele Identifier: CA2614645986
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585195_67585196insTTTTTTTTTTAATGATAC , CM000673.2:g.67585195_67585196insTTTTTTTTTTAATGATAC GRCh38
NC_000011.9:g.67352666_67352667insTTTTTTTTTTAATGATAC , CM000673.1:g.67352666_67352667insTTTTTTTTTTAATGATAC GRCh37
NC_000011.8:g.67109242_67109243insTTTTTTTTTTAATGATAC NCBI36
NG_012075.1:g.6601_6602insTTTTTTTTTTAATGATAC , LRG_723:g.6601_6602insTTTTTTTTTTAATGATAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.290_291insTTTTTTTTTTAATGATAC ENSP00000381604.1:p.Val97_Glu98insPhePhePheAsnAspThr
ENST00000398606.10:c.290_291insTTTTTTTTTTAATGATAC MANE Select ENSP00000381607.3:p.Val97_Glu98insPhePhePheAsnAspThr
ENST00000646888.1:c.*6_*7insTTTTTTTTTTAATGATAC ENSP00000494477.1:n.*6_*7insTTTTTTTTTTAATGATAC
ENST00000398603.5:c.290_291insTTTTTTTTTTAATGATAC ENSP00000381604.1:p.Val97_Glu98insPhePhePheAsnAspThr
ENST00000398606.7:c.290_291insTTTTTTTTTTAATGATAC ENSP00000381607.3:p.Val97_Glu98insPhePhePheAsnAspThr
ENST00000467591.1:n.401_402insTTTTTTTTTTAATGATAC
ENST00000494593.1:n.1085_1086insTTTTTTTTTTAATGATAC
ENST00000498765.5:c.353_354insTTTTTTTTTTAATGATAC
NM_000852.3:c.290_291insTTTTTTTTTTAATGATAC , LRG_723t1:c.290_291insTTTTTTTTTTAATGATAC NP_000843.1:p.Val97_Glu98insPhePhePheAsnAspThr
NM_000852.4:c.290_291insTTTTTTTTTTAATGATAC MANE Select NP_000843.1:p.Val97_Glu98insPhePhePheAsnAspThr