Canonical Allele Identifier: CA414705399
Gene: GPC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.132887655A>G (hg19) chrX:g.133753628A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.133753628A>G , CM000685.2:g.133753628A>G GRCh38
NC_000023.10:g.132887655A>G , CM000685.1:g.132887655A>G GRCh37
NC_000023.9:g.132715321A>G NCBI36
NG_009286.1:g.237012T>C , LRG_505:g.237012T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000406757.3:c.75T>C
ENST00000684880.1:c.*474T>C ENSP00000510280.1:n.*474T>C
ENST00000689310.1:c.838T>C ENSP00000510438.1:p.Trp280Arg
ENST00000692084.1:c.80T>C
ENST00000370818.8:c.886T>C MANE Select ENSP00000359854.3:p.Trp296Arg
ENST00000394299.7:c.886T>C ENSP00000377836.2:p.Trp296Arg
ENST00000666673.1:n.80T>C
ENST00000370818.7:c.886T>C ENSP00000359854.3:p.Trp296Arg
ENST00000394299.6:c.886T>C ENSP00000377836.2:p.Trp296Arg
ENST00000406757.2:c.75T>C
ENST00000631057.2:c.724T>C ENSP00000486325.1:p.Trp242Arg
NM_001164617.1:c.886T>C NP_001158089.1:p.Trp296Arg
NM_001164618.1:c.838T>C NP_001158090.1:p.Trp280Arg
NM_001164619.1:c.724T>C NP_001158091.1:p.Trp242Arg
NM_004484.3:c.886T>C , LRG_505t1:c.886T>C NP_004475.1:p.Trp296Arg
XM_017029413.2:c.886T>C XP_016884902.1:p.Trp296Arg
NM_001164617.2:c.886T>C NP_001158089.1:p.Trp296Arg
NM_001164618.2:c.838T>C NP_001158090.1:p.Trp280Arg
NM_001164619.2:c.724T>C NP_001158091.1:p.Trp242Arg
NM_004484.4:c.886T>C MANE Select NP_004475.1:p.Trp296Arg
Search 100 bp 5'
Search 100 bp 3'