Canonical Allele Identifier: CA2792515092

Gene: GSTP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67585199_67585200insTTTTTCAAT , CM000673.2:g.67585199_67585200insTTTTTCAAT	GRCh38
NC_000011.9:g.67352670_67352671insTTTTTCAAT , CM000673.1:g.67352670_67352671insTTTTTCAAT	GRCh37
NC_000011.8:g.67109246_67109247insTTTTTCAAT	NCBI36
NG_012075.1:g.6605_6606insTTTTTCAAT , LRG_723:g.6605_6606insTTTTTCAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.294_295insTTTTTCAAT	ENSP00000381604.1:p.Glu98_Asp99insPhePheAsn
ENST00000398606.10:c.294_295insTTTTTCAAT MANE Select	ENSP00000381607.3:p.Glu98_Asp99insPhePheAsn
ENST00000646888.1:c.*10_*11insTTTTTCAAT	ENSP00000494477.1:n.*10_*11insTTTTTCAAT
ENST00000398603.5:c.294_295insTTTTTCAAT	ENSP00000381604.1:p.Glu98_Asp99insPhePheAsn
ENST00000398606.7:c.294_295insTTTTTCAAT	ENSP00000381607.3:p.Glu98_Asp99insPhePheAsn
ENST00000467591.1:n.405_406insTTTTTCAAT
ENST00000494593.1:n.1089_1090insTTTTTCAAT
ENST00000498765.5:c.357_358insTTTTTCAAT
NM_000852.3:c.294_295insTTTTTCAAT , LRG_723t1:c.294_295insTTTTTCAAT	NP_000843.1:p.Glu98_Asp99insPhePheAsn
NM_000852.4:c.294_295insTTTTTCAAT MANE Select	NP_000843.1:p.Glu98_Asp99insPhePheAsn