Canonical Allele Identifier: CA644545035

Gene: GPC3

Linked Data

• dbSNP Id: rs1360778879
• gnomAD v2: X-133086976-G-T
• gnomAD v3: X-133952949-G-T
• gnomAD v4: X-133952949-G-T
• MyVariant Identifiers: chrX:g.133086976G>T (hg19) ; chrX:g.133952949G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133952949G>T , CM000685.2:g.133952949G>T	GRCh38
NC_000023.10:g.133086976G>T , CM000685.1:g.133086976G>T	GRCh37
NC_000023.9:g.132914642G>T	NCBI36
NG_009286.1:g.37691C>A , LRG_505:g.37691C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684880.1:c.337+101C>A	ENSP00000510280.1:n.337+101C>A
ENST00000689310.1:c.289+149C>A	ENSP00000510438.1:n.289+149C>A
ENST00000692630.1:n.467+101C>A
ENST00000370818.8:c.337+101C>A MANE Select	ENSP00000359854.3:n.337+101C>A
ENST00000394299.7:c.337+101C>A	ENSP00000377836.2:n.337+101C>A
ENST00000370818.7:c.337+101C>A	ENSP00000359854.3:n.337+101C>A
ENST00000394299.6:c.337+101C>A	ENSP00000377836.2:n.337+101C>A
ENST00000631057.2:c.175+32326C>A	ENSP00000486325.1:n.175+32326C>A
NM_001164617.1:c.337+101C>A	NP_001158089.1:n.337+101C>A
NM_001164618.1:c.289+149C>A	NP_001158090.1:n.289+149C>A
NM_001164619.1:c.175+32326C>A	NP_001158091.1:n.175+32326C>A
NM_004484.3:c.337+101C>A , LRG_505t1:c.337+101C>A	NP_004475.1:n.337+101C>A
XM_017029413.2:c.337+101C>A	XP_016884902.1:n.337+101C>A
NM_001164617.2:c.337+101C>A	NP_001158089.1:n.337+101C>A
NM_001164618.2:c.289+149C>A	NP_001158090.1:n.289+149C>A
NM_001164619.2:c.175+32326C>A	NP_001158091.1:n.175+32326C>A
NM_004484.4:c.337+101C>A MANE Select	NP_004475.1:n.337+101C>A