Canonical Allele Identifier: CA414705700

Gene: GPC3

Linked Data

• MyVariant Identifiers: chrX:g.132887724G>A (hg19) ; chrX:g.133753697G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753697G>A , CM000685.2:g.133753697G>A	GRCh38
NC_000023.10:g.132887724G>A , CM000685.1:g.132887724G>A	GRCh37
NC_000023.9:g.132715390G>A	NCBI36
NG_009286.1:g.236943C>T , LRG_505:g.236943C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406757.3:c.6C>T
ENST00000684880.1:c.*405C>T	ENSP00000510280.1:n.*405C>T
ENST00000689310.1:c.769C>T	ENSP00000510438.1:p.Pro257Ser
ENST00000692084.1:c.11C>T
ENST00000370818.8:c.817C>T MANE Select	ENSP00000359854.3:p.Pro273Ser
ENST00000394299.7:c.817C>T	ENSP00000377836.2:p.Pro273Ser
ENST00000666673.1:n.11C>T
ENST00000370818.7:c.817C>T	ENSP00000359854.3:p.Pro273Ser
ENST00000394299.6:c.817C>T	ENSP00000377836.2:p.Pro273Ser
ENST00000406757.2:c.6C>T
ENST00000631057.2:c.655C>T	ENSP00000486325.1:p.Pro219Ser
NM_001164617.1:c.817C>T	NP_001158089.1:p.Pro273Ser
NM_001164618.1:c.769C>T	NP_001158090.1:p.Pro257Ser
NM_001164619.1:c.655C>T	NP_001158091.1:p.Pro219Ser
NM_004484.3:c.817C>T , LRG_505t1:c.817C>T	NP_004475.1:p.Pro273Ser
XM_017029413.2:c.817C>T	XP_016884902.1:p.Pro273Ser
NM_001164617.2:c.817C>T	NP_001158089.1:p.Pro273Ser
NM_001164618.2:c.769C>T	NP_001158090.1:p.Pro257Ser
NM_001164619.2:c.655C>T	NP_001158091.1:p.Pro219Ser
NM_004484.4:c.817C>T MANE Select	NP_004475.1:p.Pro273Ser