Canonical Allele Identifier: CA2459438226

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133536038A= , CM000685.2:g.133536038A=	GRCh38
NC_000023.10:g.132670066A= , CM000685.1:g.132670066A=	GRCh37
NC_000023.9:g.132497732A=	NCBI36
NG_009286.1:g.454601T= , LRG_505:g.454601T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689310.1:c.*86T=	ENSP00000510438.1:n.*86T=
ENST00000370818.8:c.*86T= MANE Select	ENSP00000359854.3:n.*86T=
ENST00000394299.7:c.*86T=	ENSP00000377836.2:n.*86T=
ENST00000669691.1:n.895T=
ENST00000370818.7:c.*86T=	ENSP00000359854.3:n.*86T=
ENST00000394299.6:c.*86T=	ENSP00000377836.2:n.*86T=
NM_001164617.1:c.*86T=	NP_001158089.1:n.*86T=
NM_001164618.1:c.*86T=	NP_001158090.1:n.*86T=
NM_001164619.1:c.*86T=	NP_001158091.1:n.*86T=
NM_004484.3:c.*86T= , LRG_505t1:c.*86T=	NP_004475.1:n.*86T=
NM_001164617.2:c.*86T=	NP_001158089.1:n.*86T=
NM_001164618.2:c.*86T=	NP_001158090.1:n.*86T=
NM_001164619.2:c.*86T=	NP_001158091.1:n.*86T=
NM_004484.4:c.*86T= MANE Select	NP_004475.1:n.*86T=