Canonical Allele Identifier: CA2695236006

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753837del , CM000685.2:g.133753837del	GRCh38
NC_000023.10:g.132887864del , CM000685.1:g.132887864del	GRCh37
NC_000023.9:g.132715530del	NCBI36
NG_009286.1:g.236803del , LRG_505:g.236803del

Transcript Alleles

HGVS	Amino-acid change
ENST00000684880.1:c.*265del	ENSP00000510280.1:n.*265del
ENST00000689310.1:c.629del	ENSP00000510438.1:p.Thr210IlefsTer8
ENST00000370818.8:c.677del MANE Select	ENSP00000359854.3:p.Thr226IlefsTer8
ENST00000394299.7:c.677del	ENSP00000377836.2:p.Thr226IlefsTer8
ENST00000370818.7:c.677del	ENSP00000359854.3:p.Thr226IlefsTer8
ENST00000394299.6:c.677del	ENSP00000377836.2:p.Thr226IlefsTer8
ENST00000631057.2:c.515del	ENSP00000486325.1:p.Thr172IlefsTer8
NM_001164617.1:c.677del	NP_001158089.1:p.Thr226IlefsTer8
NM_001164618.1:c.629del	NP_001158090.1:p.Thr210IlefsTer8
NM_001164619.1:c.515del	NP_001158091.1:p.Thr172IlefsTer8
NM_004484.3:c.677del , LRG_505t1:c.677del	NP_004475.1:p.Thr226IlefsTer8
XM_017029413.2:c.677del	XP_016884902.1:p.Thr226IlefsTer8
NM_001164617.2:c.677del	NP_001158089.1:p.Thr226IlefsTer8
NM_001164618.2:c.629del	NP_001158090.1:p.Thr210IlefsTer8
NM_001164619.2:c.515del	NP_001158091.1:p.Thr172IlefsTer8
NM_004484.4:c.677del MANE Select	NP_004475.1:p.Thr226IlefsTer8