Canonical Allele Identifier: CA414705682

Gene: GPC3

Linked Data

• MyVariant Identifiers: chrX:g.132887719A>T (hg19) ; chrX:g.133753692A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753692A>T , CM000685.2:g.133753692A>T	GRCh38
NC_000023.10:g.132887719A>T , CM000685.1:g.132887719A>T	GRCh37
NC_000023.9:g.132715385A>T	NCBI36
NG_009286.1:g.236948T>A , LRG_505:g.236948T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406757.3:c.11T>A
ENST00000684880.1:c.*410T>A	ENSP00000510280.1:n.*410T>A
ENST00000689310.1:c.774T>A	ENSP00000510438.1:p.Cys258Ter
ENST00000692084.1:c.16T>A
ENST00000370818.8:c.822T>A MANE Select	ENSP00000359854.3:p.Cys274Ter
ENST00000394299.7:c.822T>A	ENSP00000377836.2:p.Cys274Ter
ENST00000666673.1:n.16T>A
ENST00000370818.7:c.822T>A	ENSP00000359854.3:p.Cys274Ter
ENST00000394299.6:c.822T>A	ENSP00000377836.2:p.Cys274Ter
ENST00000406757.2:c.11T>A
ENST00000631057.2:c.660T>A	ENSP00000486325.1:p.Cys220Ter
NM_001164617.1:c.822T>A	NP_001158089.1:p.Cys274Ter
NM_001164618.1:c.774T>A	NP_001158090.1:p.Cys258Ter
NM_001164619.1:c.660T>A	NP_001158091.1:p.Cys220Ter
NM_004484.3:c.822T>A , LRG_505t1:c.822T>A	NP_004475.1:p.Cys274Ter
XM_017029413.2:c.822T>A	XP_016884902.1:p.Cys274Ter
NM_001164617.2:c.822T>A	NP_001158089.1:p.Cys274Ter
NM_001164618.2:c.774T>A	NP_001158090.1:p.Cys258Ter
NM_001164619.2:c.660T>A	NP_001158091.1:p.Cys220Ter
NM_004484.4:c.822T>A MANE Select	NP_004475.1:p.Cys274Ter