Canonical Allele Identifier: CA2695236007

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753907_133753926del , CM000685.2:g.133753907_133753926del	GRCh38
NC_000023.10:g.132887934_132887953del , CM000685.1:g.132887934_132887953del	GRCh37
NC_000023.9:g.132715600_132715619del	NCBI36
NG_009286.1:g.236717_236736del , LRG_505:g.236717_236736del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684880.1:c.*179_*198del	ENSP00000510280.1:n.*179_*198del
ENST00000689310.1:c.543_562del	ENSP00000510438.1:p.Cys181Ter
ENST00000370818.8:c.591_610del MANE Select	ENSP00000359854.3:p.Cys197Ter
ENST00000394299.7:c.591_610del	ENSP00000377836.2:p.Cys197Ter
ENST00000370818.7:c.591_610del	ENSP00000359854.3:p.Cys197Ter
ENST00000394299.6:c.591_610del	ENSP00000377836.2:p.Cys197Ter
ENST00000631057.2:c.429_448del	ENSP00000486325.1:p.Cys143Ter
NM_001164617.1:c.591_610del	NP_001158089.1:p.Cys197Ter
NM_001164618.1:c.543_562del	NP_001158090.1:p.Cys181Ter
NM_001164619.1:c.429_448del	NP_001158091.1:p.Cys143Ter
NM_004484.3:c.591_610del , LRG_505t1:c.591_610del	NP_004475.1:p.Cys197Ter
XM_017029413.2:c.591_610del	XP_016884902.1:p.Cys197Ter
NM_001164617.2:c.591_610del	NP_001158089.1:p.Cys197Ter
NM_001164618.2:c.543_562del	NP_001158090.1:p.Cys181Ter
NM_001164619.2:c.429_448del	NP_001158091.1:p.Cys143Ter
NM_004484.4:c.591_610del MANE Select	NP_004475.1:p.Cys197Ter