Canonical Allele Identifier: CA414705490

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133753649C>T , CM000685.2:g.133753649C>T	GRCh38
NC_000023.10:g.132887676C>T , CM000685.1:g.132887676C>T	GRCh37
NC_000023.9:g.132715342C>T	NCBI36
NG_009286.1:g.236991G>A , LRG_505:g.236991G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406757.3:c.54G>A
ENST00000684880.1:c.*453G>A	ENSP00000510280.1:n.*453G>A
ENST00000689310.1:c.817G>A	ENSP00000510438.1:p.Val273Met
ENST00000692084.1:c.59G>A
ENST00000370818.8:c.865G>A MANE Select	ENSP00000359854.3:p.Val289Met
ENST00000394299.7:c.865G>A	ENSP00000377836.2:p.Val289Met
ENST00000666673.1:n.59G>A
ENST00000370818.7:c.865G>A	ENSP00000359854.3:p.Val289Met
ENST00000394299.6:c.865G>A	ENSP00000377836.2:p.Val289Met
ENST00000406757.2:c.54G>A
ENST00000631057.2:c.703G>A	ENSP00000486325.1:p.Val235Met
NM_001164617.1:c.865G>A	NP_001158089.1:p.Val289Met
NM_001164618.1:c.817G>A	NP_001158090.1:p.Val273Met
NM_001164619.1:c.703G>A	NP_001158091.1:p.Val235Met
NM_004484.3:c.865G>A , LRG_505t1:c.865G>A	NP_004475.1:p.Val289Met
XM_017029413.2:c.865G>A	XP_016884902.1:p.Val289Met
NM_001164617.2:c.865G>A	NP_001158089.1:p.Val289Met
NM_001164618.2:c.817G>A	NP_001158090.1:p.Val273Met
NM_001164619.2:c.703G>A	NP_001158091.1:p.Val235Met
NM_004484.4:c.865G>A MANE Select	NP_004475.1:p.Val289Met