Canonical Allele Identifier: CA2459438263

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133536120G= , CM000685.2:g.133536120G=	GRCh38
NC_000023.10:g.132670148G= , CM000685.1:g.132670148G=	GRCh37
NC_000023.9:g.132497814G=	NCBI36
NG_009286.1:g.454519C= , LRG_505:g.454519C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689310.1:c.*4C=	ENSP00000510438.1:n.*4C=
ENST00000370818.8:c.*4C= MANE Select	ENSP00000359854.3:n.*4C=
ENST00000394299.7:c.*4C=	ENSP00000377836.2:n.*4C=
ENST00000669691.1:n.813C=
ENST00000370818.7:c.*4C=	ENSP00000359854.3:n.*4C=
ENST00000394299.6:c.*4C=	ENSP00000377836.2:n.*4C=
NM_001164617.1:c.*4C=	NP_001158089.1:n.*4C=
NM_001164618.1:c.*4C=	NP_001158090.1:n.*4C=
NM_001164619.1:c.*4C=	NP_001158091.1:n.*4C=
NM_004484.3:c.*4C= , LRG_505t1:c.*4C=	NP_004475.1:n.*4C=
NM_001164617.2:c.*4C=	NP_001158089.1:n.*4C=
NM_001164618.2:c.*4C=	NP_001158090.1:n.*4C=
NM_001164619.2:c.*4C=	NP_001158091.1:n.*4C=
NM_004484.4:c.*4C= MANE Select	NP_004475.1:n.*4C=