Canonical Allele Identifier: CA2459564402

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133952947_133952950delinsATGC , CM000685.2:g.133952947_133952950delinsATGC	GRCh38
NC_000023.10:g.133086974_133086977delinsATGC , CM000685.1:g.133086974_133086977delinsATGC	GRCh37
NC_000023.9:g.132914640_132914643delinsATGC	NCBI36
NG_009286.1:g.37690_37693delinsGCAT , LRG_505:g.37690_37693delinsGCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684880.1:c.337+100_337+103delinsGCAT	ENSP00000510280.1:n.337+100_337+103delinsGCAT
ENST00000689310.1:c.289+148_289+151delinsGCAT	ENSP00000510438.1:n.289+148_289+151delinsGCAT
ENST00000692630.1:n.467+100_467+103delinsGCAT
ENST00000370818.8:c.337+100_337+103delinsGCAT MANE Select	ENSP00000359854.3:n.337+100_337+103delinsGCAT
ENST00000394299.7:c.337+100_337+103delinsGCAT	ENSP00000377836.2:n.337+100_337+103delinsGCAT
ENST00000370818.7:c.337+100_337+103delinsGCAT	ENSP00000359854.3:n.337+100_337+103delinsGCAT
ENST00000394299.6:c.337+100_337+103delinsGCAT	ENSP00000377836.2:n.337+100_337+103delinsGCAT
ENST00000631057.2:c.175+32325_175+32328delinsGCAT	ENSP00000486325.1:n.175+32325_175+32328delinsGCAT
NM_001164617.1:c.337+100_337+103delinsGCAT	NP_001158089.1:n.337+100_337+103delinsGCAT
NM_001164618.1:c.289+148_289+151delinsGCAT	NP_001158090.1:n.289+148_289+151delinsGCAT
NM_001164619.1:c.175+32325_175+32328delinsGCAT	NP_001158091.1:n.175+32325_175+32328delinsGCAT
NM_004484.3:c.337+100_337+103delinsGCAT , LRG_505t1:c.337+100_337+103delinsGCAT	NP_004475.1:n.337+100_337+103delinsGCAT
XM_017029413.2:c.337+100_337+103delinsGCAT	XP_016884902.1:n.337+100_337+103delinsGCAT
NM_001164617.2:c.337+100_337+103delinsGCAT	NP_001158089.1:n.337+100_337+103delinsGCAT
NM_001164618.2:c.289+148_289+151delinsGCAT	NP_001158090.1:n.289+148_289+151delinsGCAT
NM_001164619.2:c.175+32325_175+32328delinsGCAT	NP_001158091.1:n.175+32325_175+32328delinsGCAT
NM_004484.4:c.337+100_337+103delinsGCAT MANE Select	NP_004475.1:n.337+100_337+103delinsGCAT