Canonical Allele Identifier: CA2459503322

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753898T= , CM000685.2:g.133753898T=	GRCh38
NC_000023.10:g.132887925T= , CM000685.1:g.132887925T=	GRCh37
NC_000023.9:g.132715591T=	NCBI36
NG_009286.1:g.236742A= , LRG_505:g.236742A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684880.1:c.*204A=	ENSP00000510280.1:n.*204A=
ENST00000689310.1:c.568A=	ENSP00000510438.1:p.Lys190=
ENST00000370818.8:c.616A= MANE Select	ENSP00000359854.3:p.Lys206=
ENST00000394299.7:c.616A=	ENSP00000377836.2:p.Lys206=
ENST00000370818.7:c.616A=	ENSP00000359854.3:p.Lys206=
ENST00000394299.6:c.616A=	ENSP00000377836.2:p.Lys206=
ENST00000631057.2:c.454A=	ENSP00000486325.1:p.Lys152=
NM_001164617.1:c.616A=	NP_001158089.1:p.Lys206=
NM_001164618.1:c.568A=	NP_001158090.1:p.Lys190=
NM_001164619.1:c.454A=	NP_001158091.1:p.Lys152=
NM_004484.3:c.616A= , LRG_505t1:c.616A=	NP_004475.1:p.Lys206=
XM_017029413.2:c.616A=	XP_016884902.1:p.Lys206=
NM_001164617.2:c.616A=	NP_001158089.1:p.Lys206=
NM_001164618.2:c.568A=	NP_001158090.1:p.Lys190=
NM_001164619.2:c.454A=	NP_001158091.1:p.Lys152=
NM_004484.4:c.616A= MANE Select	NP_004475.1:p.Lys206=