Canonical Allele Identifier: CA2459503278

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753743G= , CM000685.2:g.133753743G=	GRCh38
NC_000023.10:g.132887770G= , CM000685.1:g.132887770G=	GRCh37
NC_000023.9:g.132715436G=	NCBI36
NG_009286.1:g.236897C= , LRG_505:g.236897C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000684880.1:c.*359C=	ENSP00000510280.1:n.*359C=
ENST00000689310.1:c.723C=	ENSP00000510438.1:p.Thr241=
ENST00000370818.8:c.771C= MANE Select	ENSP00000359854.3:p.Thr257=
ENST00000394299.7:c.771C=	ENSP00000377836.2:p.Thr257=
ENST00000370818.7:c.771C=	ENSP00000359854.3:p.Thr257=
ENST00000394299.6:c.771C=	ENSP00000377836.2:p.Thr257=
ENST00000631057.2:c.609C=	ENSP00000486325.1:p.Thr203=
NM_001164617.1:c.771C=	NP_001158089.1:p.Thr257=
NM_001164618.1:c.723C=	NP_001158090.1:p.Thr241=
NM_001164619.1:c.609C=	NP_001158091.1:p.Thr203=
NM_004484.3:c.771C= , LRG_505t1:c.771C=	NP_004475.1:p.Thr257=
XM_017029413.2:c.771C=	XP_016884902.1:p.Thr257=
NM_001164617.2:c.771C=	NP_001158089.1:p.Thr257=
NM_001164618.2:c.723C=	NP_001158090.1:p.Thr241=
NM_001164619.2:c.609C=	NP_001158091.1:p.Thr203=
NM_004484.4:c.771C= MANE Select	NP_004475.1:p.Thr257=