Canonical Allele Identifier: CA599909378

Gene: GSTP1

Linked Data

• dbSNP Id: rs1456281907
• gnomAD v2: 11-67352670-G-GTTTTTTAAT
• gnomAD v3: 11-67585199-G-GTTTTTTAAT
• gnomAD v4: 11-67585199-G-GTTTTTTAAT
• MyVariant Identifiers: chr11:g.67352670_67352671insTTTTTTAAT (hg19) ; chr11:g.67585199_67585200insTTTTTTAAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67585199_67585200insTTTTTTAAT , CM000673.2:g.67585199_67585200insTTTTTTAAT	GRCh38
NC_000011.9:g.67352670_67352671insTTTTTTAAT , CM000673.1:g.67352670_67352671insTTTTTTAAT	GRCh37
NC_000011.8:g.67109246_67109247insTTTTTTAAT	NCBI36
NG_012075.1:g.6605_6606insTTTTTTAAT , LRG_723:g.6605_6606insTTTTTTAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.294_295insTTTTTTAAT	ENSP00000381604.1:p.Glu98_Asp99insPhePheAsn
ENST00000398606.10:c.294_295insTTTTTTAAT MANE Select	ENSP00000381607.3:p.Glu98_Asp99insPhePheAsn
ENST00000646888.1:c.*10_*11insTTTTTTAAT	ENSP00000494477.1:n.*10_*11insTTTTTTAAT
ENST00000398603.5:c.294_295insTTTTTTAAT	ENSP00000381604.1:p.Glu98_Asp99insPhePheAsn
ENST00000398606.7:c.294_295insTTTTTTAAT	ENSP00000381607.3:p.Glu98_Asp99insPhePheAsn
ENST00000467591.1:n.405_406insTTTTTTAAT
ENST00000494593.1:n.1089_1090insTTTTTTAAT
ENST00000498765.5:c.357_358insTTTTTTAAT
NM_000852.3:c.294_295insTTTTTTAAT , LRG_723t1:c.294_295insTTTTTTAAT	NP_000843.1:p.Glu98_Asp99insPhePheAsn
NM_000852.4:c.294_295insTTTTTTAAT MANE Select	NP_000843.1:p.Glu98_Asp99insPhePheAsn