Canonical Allele Identifier: CA871716630

Gene: GPC3

Linked Data

• dbSNP Id: rs1268628286
• gnomAD v3: X-133536050-TA-T
• gnomAD v4: X-133536050-TA-T
• MyVariant Identifiers: chrX:g.132670079del (hg19) ; chrX:g.133536051del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.133536052del , CM000685.2:g.133536052del	GRCh38
NC_000023.10:g.132670080del , CM000685.1:g.132670080del	GRCh37
NC_000023.9:g.132497746del	NCBI36
NG_009286.1:g.454588del , LRG_505:g.454588del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689310.1:c.*73del	ENSP00000510438.1:n.*73del
ENST00000370818.8:c.*73del MANE Select	ENSP00000359854.3:n.*73del
ENST00000394299.7:c.*73del	ENSP00000377836.2:n.*73del
ENST00000669691.1:n.882del
ENST00000370818.7:c.*73del	ENSP00000359854.3:n.*73del
ENST00000394299.6:c.*73del	ENSP00000377836.2:n.*73del
NM_001164617.1:c.*73del	NP_001158089.1:n.*73del
NM_001164618.1:c.*73del	NP_001158090.1:n.*73del
NM_001164619.1:c.*73del	NP_001158091.1:n.*73del
NM_004484.3:c.*73del , LRG_505t1:c.*73del	NP_004475.1:n.*73del
NM_001164617.2:c.*73del	NP_001158089.1:n.*73del
NM_001164618.2:c.*73del	NP_001158090.1:n.*73del
NM_001164619.2:c.*73del	NP_001158091.1:n.*73del
NM_004484.4:c.*73del MANE Select	NP_004475.1:n.*73del