Canonical Allele Identifier: CA2579705752

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133985190del , CM000685.2:g.133985190del	GRCh38
NC_000023.10:g.133119217del , CM000685.1:g.133119217del	GRCh37
NC_000023.9:g.132946883del	NCBI36
NG_009286.1:g.5450del , LRG_505:g.5450del

Transcript Alleles

HGVS	Amino-acid change
ENST00000684880.1:c.175+85del	ENSP00000510280.1:n.175+85del
ENST00000689310.1:c.175+85del	ENSP00000510438.1:n.175+85del
ENST00000692630.1:n.305+85del
ENST00000370818.8:c.175+85del MANE Select	ENSP00000359854.3:n.175+85del
ENST00000394299.7:c.175+85del	ENSP00000377836.2:n.175+85del
ENST00000370818.7:c.175+85del	ENSP00000359854.3:n.175+85del
ENST00000394299.6:c.175+85del	ENSP00000377836.2:n.175+85del
ENST00000631057.2:c.175+85del	ENSP00000486325.1:n.175+85del
NM_001164617.1:c.175+85del	NP_001158089.1:n.175+85del
NM_001164618.1:c.175+85del	NP_001158090.1:n.175+85del
NM_001164619.1:c.175+85del	NP_001158091.1:n.175+85del
NM_004484.3:c.175+85del , LRG_505t1:c.175+85del	NP_004475.1:n.175+85del
XM_017029413.2:c.175+85del	XP_016884902.1:n.175+85del
NM_001164617.2:c.175+85del	NP_001158089.1:n.175+85del
NM_001164618.2:c.175+85del	NP_001158090.1:n.175+85del
NM_001164619.2:c.175+85del	NP_001158091.1:n.175+85del
NM_004484.4:c.175+85del MANE Select	NP_004475.1:n.175+85del