Canonical Allele Identifier: CA2459503305
Gene: GPC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.133753841C= , CM000685.2:g.133753841C= GRCh38
NC_000023.10:g.132887868C= , CM000685.1:g.132887868C= GRCh37
NC_000023.9:g.132715534C= NCBI36
NG_009286.1:g.236799G= , LRG_505:g.236799G=

Transcript Alleles

HGVS Amino-acid change
ENST00000684880.1:c.*261G= ENSP00000510280.1:n.*261G=
ENST00000689310.1:c.625G= ENSP00000510438.1:p.Val209=
ENST00000370818.8:c.673G= MANE Select ENSP00000359854.3:p.Val225=
ENST00000394299.7:c.673G= ENSP00000377836.2:p.Val225=
ENST00000370818.7:c.673G= ENSP00000359854.3:p.Val225=
ENST00000394299.6:c.673G= ENSP00000377836.2:p.Val225=
ENST00000631057.2:c.511G= ENSP00000486325.1:p.Val171=
NM_001164617.1:c.673G= NP_001158089.1:p.Val225=
NM_001164618.1:c.625G= NP_001158090.1:p.Val209=
NM_001164619.1:c.511G= NP_001158091.1:p.Val171=
NM_004484.3:c.673G= , LRG_505t1:c.673G= NP_004475.1:p.Val225=
XM_017029413.2:c.673G= XP_016884902.1:p.Val225=
NM_001164617.2:c.673G= NP_001158089.1:p.Val225=
NM_001164618.2:c.625G= NP_001158090.1:p.Val209=
NM_001164619.2:c.511G= NP_001158091.1:p.Val171=
NM_004484.4:c.673G= MANE Select NP_004475.1:p.Val225=