Canonical Allele Identifier: CA871694642

Gene: GPC3

Linked Data

• dbSNP Id: rs1178994397
• gnomAD v3: X-133754236-A-G
• gnomAD v4: X-133754236-A-G
• MyVariant Identifiers: chrX:g.132888263A>G (hg19) ; chrX:g.133754236A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133754236A>G , CM000685.2:g.133754236A>G	GRCh38
NC_000023.10:g.132888263A>G , CM000685.1:g.132888263A>G	GRCh37
NC_000023.9:g.132715929A>G	NCBI36
NG_009286.1:g.236404T>C , LRG_505:g.236404T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684880.1:c.409-60T>C	ENSP00000510280.1:n.409-60T>C
ENST00000689310.1:c.290-60T>C	ENSP00000510438.1:n.290-60T>C
ENST00000692630.1:n.468-60T>C
ENST00000370818.8:c.338-60T>C MANE Select	ENSP00000359854.3:n.338-60T>C
ENST00000394299.7:c.338-60T>C	ENSP00000377836.2:n.338-60T>C
ENST00000370818.7:c.338-60T>C	ENSP00000359854.3:n.338-60T>C
ENST00000394299.6:c.338-60T>C	ENSP00000377836.2:n.338-60T>C
ENST00000631057.2:c.176-60T>C	ENSP00000486325.1:n.176-60T>C
NM_001164617.1:c.338-60T>C	NP_001158089.1:n.338-60T>C
NM_001164618.1:c.290-60T>C	NP_001158090.1:n.290-60T>C
NM_001164619.1:c.176-60T>C	NP_001158091.1:n.176-60T>C
NM_004484.3:c.338-60T>C , LRG_505t1:c.338-60T>C	NP_004475.1:n.338-60T>C
XM_017029413.2:c.338-60T>C	XP_016884902.1:n.338-60T>C
NM_001164617.2:c.338-60T>C	NP_001158089.1:n.338-60T>C
NM_001164618.2:c.290-60T>C	NP_001158090.1:n.290-60T>C
NM_001164619.2:c.176-60T>C	NP_001158091.1:n.176-60T>C
NM_004484.4:c.338-60T>C MANE Select	NP_004475.1:n.338-60T>C