Canonical Allele Identifier: CA414704252

Gene: GPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133661729C>G , CM000685.2:g.133661729C>G	GRCh38
NC_000023.10:g.132795757C>G , CM000685.1:g.132795757C>G	GRCh37
NC_000023.9:g.132623423C>G	NCBI36
NG_009286.1:g.328910G>C , LRG_505:g.328910G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406757.3:c.602+1G>C
ENST00000666673.2:n.444+1G>C
ENST00000689310.1:c.1365+1G>C	ENSP00000510438.1:n.1365+1G>C
ENST00000692074.1:n.357+1G>C
ENST00000692084.1:c.700+1G>C
ENST00000370818.8:c.1413+1G>C MANE Select	ENSP00000359854.3:n.1413+1G>C
ENST00000394299.7:c.1482+1G>C	ENSP00000377836.2:n.1482+1G>C
ENST00000666017.1:n.291+1G>C
ENST00000666673.1:n.700+1G>C
ENST00000667662.1:n.480+1G>C
ENST00000669691.1:n.479+1G>C
ENST00000370818.7:c.1413+1G>C	ENSP00000359854.3:n.1413+1G>C
ENST00000394299.6:c.1482+1G>C	ENSP00000377836.2:n.1482+1G>C
ENST00000406757.2:c.602+1G>C
ENST00000631057.2:c.1251+1G>C	ENSP00000486325.1:n.1251+1G>C
NM_001164617.1:c.1482+1G>C	NP_001158089.1:n.1482+1G>C
NM_001164618.1:c.1365+1G>C	NP_001158090.1:n.1365+1G>C
NM_001164619.1:c.1251+1G>C	NP_001158091.1:n.1251+1G>C
NM_004484.3:c.1413+1G>C , LRG_505t1:c.1413+1G>C	NP_004475.1:n.1413+1G>C
NM_001164617.2:c.1482+1G>C	NP_001158089.1:n.1482+1G>C
NM_001164618.2:c.1365+1G>C	NP_001158090.1:n.1365+1G>C
NM_001164619.2:c.1251+1G>C	NP_001158091.1:n.1251+1G>C
NM_004484.4:c.1413+1G>C MANE Select	NP_004475.1:n.1413+1G>C