Canonical Allele Identifier: CA2694733028
Gene: GPC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.133754197_133754199del , CM000685.2:g.133754197_133754199del GRCh38
NC_000023.10:g.132888224_132888226del , CM000685.1:g.132888224_132888226del GRCh37
NC_000023.9:g.132715890_132715892del NCBI36
NG_009286.1:g.236441_236443del , LRG_505:g.236441_236443del

Transcript Alleles

HGVS Amino-acid Change
ENST00000684880.1:c.409-23_409-21del ENSP00000510280.1:n.409-23_409-21del
ENST00000689310.1:c.290-23_290-21del ENSP00000510438.1:n.290-23_290-21del
ENST00000692630.1:n.468-23_468-21del
ENST00000370818.8:c.338-23_338-21del MANE Select ENSP00000359854.3:n.338-23_338-21del
ENST00000394299.7:c.338-23_338-21del ENSP00000377836.2:n.338-23_338-21del
ENST00000370818.7:c.338-23_338-21del ENSP00000359854.3:n.338-23_338-21del
ENST00000394299.6:c.338-23_338-21del ENSP00000377836.2:n.338-23_338-21del
ENST00000631057.2:c.176-23_176-21del ENSP00000486325.1:n.176-23_176-21del
NM_001164617.1:c.338-23_338-21del NP_001158089.1:n.338-23_338-21del
NM_001164618.1:c.290-23_290-21del NP_001158090.1:n.290-23_290-21del
NM_001164619.1:c.176-23_176-21del NP_001158091.1:n.176-23_176-21del
NM_004484.3:c.338-23_338-21del , LRG_505t1:c.338-23_338-21del NP_004475.1:n.338-23_338-21del
XM_017029413.2:c.338-23_338-21del XP_016884902.1:n.338-23_338-21del
NM_001164617.2:c.338-23_338-21del NP_001158089.1:n.338-23_338-21del
NM_001164618.2:c.290-23_290-21del NP_001158090.1:n.290-23_290-21del
NM_001164619.2:c.176-23_176-21del NP_001158091.1:n.176-23_176-21del
NM_004484.4:c.338-23_338-21del MANE Select NP_004475.1:n.338-23_338-21del