Canonical Allele Identifier: CA2459503467

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133754293G= , CM000685.2:g.133754293G=	GRCh38
NC_000023.10:g.132888320G= , CM000685.1:g.132888320G=	GRCh37
NC_000023.9:g.132715986G=	NCBI36
NG_009286.1:g.236347C= , LRG_505:g.236347C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684880.1:c.409-117C=	ENSP00000510280.1:n.409-117C=
ENST00000689310.1:c.290-117C=	ENSP00000510438.1:n.290-117C=
ENST00000692630.1:n.468-117C=
ENST00000370818.8:c.338-117C= MANE Select	ENSP00000359854.3:n.338-117C=
ENST00000394299.7:c.338-117C=	ENSP00000377836.2:n.338-117C=
ENST00000370818.7:c.338-117C=	ENSP00000359854.3:n.338-117C=
ENST00000394299.6:c.338-117C=	ENSP00000377836.2:n.338-117C=
ENST00000631057.2:c.176-117C=	ENSP00000486325.1:n.176-117C=
NM_001164617.1:c.338-117C=	NP_001158089.1:n.338-117C=
NM_001164618.1:c.290-117C=	NP_001158090.1:n.290-117C=
NM_001164619.1:c.176-117C=	NP_001158091.1:n.176-117C=
NM_004484.3:c.338-117C= , LRG_505t1:c.338-117C=	NP_004475.1:n.338-117C=
XM_017029413.2:c.338-117C=	XP_016884902.1:n.338-117C=
NM_001164617.2:c.338-117C=	NP_001158089.1:n.338-117C=
NM_001164618.2:c.290-117C=	NP_001158090.1:n.290-117C=
NM_001164619.2:c.176-117C=	NP_001158091.1:n.176-117C=
NM_004484.4:c.338-117C= MANE Select	NP_004475.1:n.338-117C=