Canonical Allele Identifier: CA939080865

Gene: GSTP1

Linked Data

• gnomAD v3: 11-67585199-G-GTTTTTTCAT
• gnomAD v4: 11-67585199-G-GTTTTTTCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67585199_67585200insTTTTTTCAT , CM000673.2:g.67585199_67585200insTTTTTTCAT	GRCh38
NC_000011.9:g.67352670_67352671insTTTTTTCAT , CM000673.1:g.67352670_67352671insTTTTTTCAT	GRCh37
NC_000011.8:g.67109246_67109247insTTTTTTCAT	NCBI36
NG_012075.1:g.6605_6606insTTTTTTCAT , LRG_723:g.6605_6606insTTTTTTCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.294_295insTTTTTTCAT	ENSP00000381604.1:p.Glu98_Asp99insPhePheHis
ENST00000398606.10:c.294_295insTTTTTTCAT MANE Select	ENSP00000381607.3:p.Glu98_Asp99insPhePheHis
ENST00000646888.1:c.*10_*11insTTTTTTCAT	ENSP00000494477.1:n.*10_*11insTTTTTTCAT
ENST00000398603.5:c.294_295insTTTTTTCAT	ENSP00000381604.1:p.Glu98_Asp99insPhePheHis
ENST00000398606.7:c.294_295insTTTTTTCAT	ENSP00000381607.3:p.Glu98_Asp99insPhePheHis
ENST00000467591.1:n.405_406insTTTTTTCAT
ENST00000494593.1:n.1089_1090insTTTTTTCAT
ENST00000498765.5:c.357_358insTTTTTTCAT
NM_000852.3:c.294_295insTTTTTTCAT , LRG_723t1:c.294_295insTTTTTTCAT	NP_000843.1:p.Glu98_Asp99insPhePheHis
NM_000852.4:c.294_295insTTTTTTCAT MANE Select	NP_000843.1:p.Glu98_Asp99insPhePheHis