Canonical Allele Identifier: CA2459487434

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133699912G= , CM000685.2:g.133699912G=	GRCh38
NC_000023.10:g.132833940G= , CM000685.1:g.132833940G=	GRCh37
NC_000023.9:g.132661606G=	NCBI36
NG_009286.1:g.290727C= , LRG_505:g.290727C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406757.3:c.338C=
ENST00000666673.2:n.180C=
ENST00000684880.1:c.*737C=	ENSP00000510280.1:n.*737C=
ENST00000689310.1:c.1101C=	ENSP00000510438.1:p.Thr367=
ENST00000692084.1:c.436C=
ENST00000370818.8:c.1149C= MANE Select	ENSP00000359854.3:p.Thr383=
ENST00000394299.7:c.1218C=	ENSP00000377836.2:p.Thr406=
ENST00000666673.1:n.436C=
ENST00000667662.1:n.216C=
ENST00000669691.1:n.195C=
ENST00000370818.7:c.1149C=	ENSP00000359854.3:p.Thr383=
ENST00000394299.6:c.1218C=	ENSP00000377836.2:p.Thr406=
ENST00000406757.2:c.338C=
ENST00000631057.2:c.987C=	ENSP00000486325.1:p.Thr329=
NM_001164617.1:c.1218C=	NP_001158089.1:p.Thr406=
NM_001164618.1:c.1101C=	NP_001158090.1:p.Thr367=
NM_001164619.1:c.987C=	NP_001158091.1:p.Thr329=
NM_004484.3:c.1149C= , LRG_505t1:c.1149C=	NP_004475.1:p.Thr383=
XM_017029413.2:c.1149C=	XP_016884902.1:p.Thr383=
NM_001164617.2:c.1218C=	NP_001158089.1:p.Thr406=
NM_001164618.2:c.1101C=	NP_001158090.1:p.Thr367=
NM_001164619.2:c.987C=	NP_001158091.1:p.Thr329=
NM_004484.4:c.1149C= MANE Select	NP_004475.1:p.Thr383=