Canonical Allele Identifier: CA414706054
Gene: GPC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.133753814T>G , CM000685.2:g.133753814T>G GRCh38
NC_000023.10:g.132887841T>G , CM000685.1:g.132887841T>G GRCh37
NC_000023.9:g.132715507T>G NCBI36
NG_009286.1:g.236826A>C , LRG_505:g.236826A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684880.1:c.*288A>C ENSP00000510280.1:n.*288A>C
ENST00000689310.1:c.652A>C ENSP00000510438.1:p.Asn218His
ENST00000370818.8:c.700A>C MANE Select ENSP00000359854.3:p.Asn234His
ENST00000394299.7:c.700A>C ENSP00000377836.2:p.Asn234His
ENST00000370818.7:c.700A>C ENSP00000359854.3:p.Asn234His
ENST00000394299.6:c.700A>C ENSP00000377836.2:p.Asn234His
ENST00000631057.2:c.538A>C ENSP00000486325.1:p.Asn180His
NM_001164617.1:c.700A>C NP_001158089.1:p.Asn234His
NM_001164618.1:c.652A>C NP_001158090.1:p.Asn218His
NM_001164619.1:c.538A>C NP_001158091.1:p.Asn180His
NM_004484.3:c.700A>C , LRG_505t1:c.700A>C NP_004475.1:p.Asn234His
XM_017029413.2:c.700A>C XP_016884902.1:p.Asn234His
NM_001164617.2:c.700A>C NP_001158089.1:p.Asn234His
NM_001164618.2:c.652A>C NP_001158090.1:p.Asn218His
NM_001164619.2:c.538A>C NP_001158091.1:p.Asn180His
NM_004484.4:c.700A>C MANE Select NP_004475.1:p.Asn234His