Canonical Allele Identifier: CA2459487430

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133699903G= , CM000685.2:g.133699903G=	GRCh38
NC_000023.10:g.132833931G= , CM000685.1:g.132833931G=	GRCh37
NC_000023.9:g.132661597G=	NCBI36
NG_009286.1:g.290736C= , LRG_505:g.290736C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406757.3:c.347C=
ENST00000666673.2:n.189C=
ENST00000684880.1:c.*746C=	ENSP00000510280.1:n.*746C=
ENST00000689310.1:c.1110C=	ENSP00000510438.1:p.Ser370=
ENST00000692084.1:c.445C=
ENST00000370818.8:c.1158C= MANE Select	ENSP00000359854.3:p.Ser386=
ENST00000394299.7:c.1227C=	ENSP00000377836.2:p.Ser409=
ENST00000666673.1:n.445C=
ENST00000667662.1:n.225C=
ENST00000669691.1:n.204C=
ENST00000370818.7:c.1158C=	ENSP00000359854.3:p.Ser386=
ENST00000394299.6:c.1227C=	ENSP00000377836.2:p.Ser409=
ENST00000406757.2:c.347C=
ENST00000631057.2:c.996C=	ENSP00000486325.1:p.Ser332=
NM_001164617.1:c.1227C=	NP_001158089.1:p.Ser409=
NM_001164618.1:c.1110C=	NP_001158090.1:p.Ser370=
NM_001164619.1:c.996C=	NP_001158091.1:p.Ser332=
NM_004484.3:c.1158C= , LRG_505t1:c.1158C=	NP_004475.1:p.Ser386=
XM_017029413.2:c.1158C=	XP_016884902.1:p.Ser386=
NM_001164617.2:c.1227C=	NP_001158089.1:p.Ser409=
NM_001164618.2:c.1110C=	NP_001158090.1:p.Ser370=
NM_001164619.2:c.996C=	NP_001158091.1:p.Ser332=
NM_004484.4:c.1158C= MANE Select	NP_004475.1:p.Ser386=