Canonical Allele Identifier: CA2459564415

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133952982T= , CM000685.2:g.133952982T=	GRCh38
NC_000023.10:g.133087009T= , CM000685.1:g.133087009T=	GRCh37
NC_000023.9:g.132914675T=	NCBI36
NG_009286.1:g.37658A= , LRG_505:g.37658A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684880.1:c.337+68A=	ENSP00000510280.1:n.337+68A=
ENST00000689310.1:c.289+116A=	ENSP00000510438.1:n.289+116A=
ENST00000692630.1:n.467+68A=
ENST00000370818.8:c.337+68A= MANE Select	ENSP00000359854.3:n.337+68A=
ENST00000394299.7:c.337+68A=	ENSP00000377836.2:n.337+68A=
ENST00000370818.7:c.337+68A=	ENSP00000359854.3:n.337+68A=
ENST00000394299.6:c.337+68A=	ENSP00000377836.2:n.337+68A=
ENST00000631057.2:c.175+32293A=	ENSP00000486325.1:n.175+32293A=
NM_001164617.1:c.337+68A=	NP_001158089.1:n.337+68A=
NM_001164618.1:c.289+116A=	NP_001158090.1:n.289+116A=
NM_001164619.1:c.175+32293A=	NP_001158091.1:n.175+32293A=
NM_004484.3:c.337+68A= , LRG_505t1:c.337+68A=	NP_004475.1:n.337+68A=
XM_017029413.2:c.337+68A=	XP_016884902.1:n.337+68A=
NM_001164617.2:c.337+68A=	NP_001158089.1:n.337+68A=
NM_001164618.2:c.289+116A=	NP_001158090.1:n.289+116A=
NM_001164619.2:c.175+32293A=	NP_001158091.1:n.175+32293A=
NM_004484.4:c.337+68A= MANE Select	NP_004475.1:n.337+68A=