Canonical Allele Identifier: CA2694733021

Gene: GPC3

Linked Data

• gnomAD v4: X-133754195-A-AAAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133754196_133754197insAAGA , CM000685.2:g.133754196_133754197insAAGA	GRCh38
NC_000023.10:g.132888223_132888224insAAGA , CM000685.1:g.132888223_132888224insAAGA	GRCh37
NC_000023.9:g.132715889_132715890insAAGA	NCBI36
NG_009286.1:g.236444_236445insCTTT , LRG_505:g.236444_236445insCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684880.1:c.409-20_409-19insCTTT	ENSP00000510280.1:n.409-20_409-19insCTTT
ENST00000689310.1:c.290-20_290-19insCTTT	ENSP00000510438.1:n.290-20_290-19insCTTT
ENST00000692630.1:n.468-20_468-19insCTTT
ENST00000370818.8:c.338-20_338-19insCTTT MANE Select	ENSP00000359854.3:n.338-20_338-19insCTTT
ENST00000394299.7:c.338-20_338-19insCTTT	ENSP00000377836.2:n.338-20_338-19insCTTT
ENST00000370818.7:c.338-20_338-19insCTTT	ENSP00000359854.3:n.338-20_338-19insCTTT
ENST00000394299.6:c.338-20_338-19insCTTT	ENSP00000377836.2:n.338-20_338-19insCTTT
ENST00000631057.2:c.176-20_176-19insCTTT	ENSP00000486325.1:n.176-20_176-19insCTTT
NM_001164617.1:c.338-20_338-19insCTTT	NP_001158089.1:n.338-20_338-19insCTTT
NM_001164618.1:c.290-20_290-19insCTTT	NP_001158090.1:n.290-20_290-19insCTTT
NM_001164619.1:c.176-20_176-19insCTTT	NP_001158091.1:n.176-20_176-19insCTTT
NM_004484.3:c.338-20_338-19insCTTT , LRG_505t1:c.338-20_338-19insCTTT	NP_004475.1:n.338-20_338-19insCTTT
XM_017029413.2:c.338-20_338-19insCTTT	XP_016884902.1:n.338-20_338-19insCTTT
NM_001164617.2:c.338-20_338-19insCTTT	NP_001158089.1:n.338-20_338-19insCTTT
NM_001164618.2:c.290-20_290-19insCTTT	NP_001158090.1:n.290-20_290-19insCTTT
NM_001164619.2:c.176-20_176-19insCTTT	NP_001158091.1:n.176-20_176-19insCTTT
NM_004484.4:c.338-20_338-19insCTTT MANE Select	NP_004475.1:n.338-20_338-19insCTTT