Canonical Allele Identifier: CA2459503382

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133754064T= , CM000685.2:g.133754064T=	GRCh38
NC_000023.10:g.132888091T= , CM000685.1:g.132888091T=	GRCh37
NC_000023.9:g.132715757T=	NCBI36
NG_009286.1:g.236576A= , LRG_505:g.236576A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684880.1:c.*38A=	ENSP00000510280.1:n.*38A=
ENST00000689310.1:c.402A=	ENSP00000510438.1:p.Thr134=
ENST00000692630.1:n.580A=
ENST00000370818.8:c.450A= MANE Select	ENSP00000359854.3:p.Thr150=
ENST00000394299.7:c.450A=	ENSP00000377836.2:p.Thr150=
ENST00000370818.7:c.450A=	ENSP00000359854.3:p.Thr150=
ENST00000394299.6:c.450A=	ENSP00000377836.2:p.Thr150=
ENST00000631057.2:c.288A=	ENSP00000486325.1:p.Thr96=
NM_001164617.1:c.450A=	NP_001158089.1:p.Thr150=
NM_001164618.1:c.402A=	NP_001158090.1:p.Thr134=
NM_001164619.1:c.288A=	NP_001158091.1:p.Thr96=
NM_004484.3:c.450A= , LRG_505t1:c.450A=	NP_004475.1:p.Thr150=
XM_017029413.2:c.450A=	XP_016884902.1:p.Thr150=
NM_001164617.2:c.450A=	NP_001158089.1:p.Thr150=
NM_001164618.2:c.402A=	NP_001158090.1:p.Thr134=
NM_001164619.2:c.288A=	NP_001158091.1:p.Thr96=
NM_004484.4:c.450A= MANE Select	NP_004475.1:p.Thr150=