Canonical Allele Identifier: CA2694733041

Gene: GPC3

Linked Data

• gnomAD v4: X-133754207-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133754207A>C , CM000685.2:g.133754207A>C	GRCh38
NC_000023.10:g.132888234A>C , CM000685.1:g.132888234A>C	GRCh37
NC_000023.9:g.132715900A>C	NCBI36
NG_009286.1:g.236433T>G , LRG_505:g.236433T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684880.1:c.409-31T>G	ENSP00000510280.1:n.409-31T>G
ENST00000689310.1:c.290-31T>G	ENSP00000510438.1:n.290-31T>G
ENST00000692630.1:n.468-31T>G
ENST00000370818.8:c.338-31T>G MANE Select	ENSP00000359854.3:n.338-31T>G
ENST00000394299.7:c.338-31T>G	ENSP00000377836.2:n.338-31T>G
ENST00000370818.7:c.338-31T>G	ENSP00000359854.3:n.338-31T>G
ENST00000394299.6:c.338-31T>G	ENSP00000377836.2:n.338-31T>G
ENST00000631057.2:c.176-31T>G	ENSP00000486325.1:n.176-31T>G
NM_001164617.1:c.338-31T>G	NP_001158089.1:n.338-31T>G
NM_001164618.1:c.290-31T>G	NP_001158090.1:n.290-31T>G
NM_001164619.1:c.176-31T>G	NP_001158091.1:n.176-31T>G
NM_004484.3:c.338-31T>G , LRG_505t1:c.338-31T>G	NP_004475.1:n.338-31T>G
XM_017029413.2:c.338-31T>G	XP_016884902.1:n.338-31T>G
NM_001164617.2:c.338-31T>G	NP_001158089.1:n.338-31T>G
NM_001164618.2:c.290-31T>G	NP_001158090.1:n.290-31T>G
NM_001164619.2:c.176-31T>G	NP_001158091.1:n.176-31T>G
NM_004484.4:c.338-31T>G MANE Select	NP_004475.1:n.338-31T>G