Canonical Allele Identifier: CA1345066382
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10142156_10142206delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG , CM000665.2:g.10142156_10142206delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG GRCh38
NC_000003.11:g.10183840_10183890delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG , CM000665.1:g.10183840_10183890delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG GRCh37
NC_000003.10:g.10158840_10158890delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG NCBI36
NG_008212.3:g.5522_5572delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG , LRG_322:g.5522_5572delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.309_340+19delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG
ENST00000696143.1:c.309_340+19delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG
ENST00000696153.1:c.309_340+19delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG
ENST00000256474.3:c.309_340+19delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG
ENST00000256474.2:c.309_340+19delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG
ENST00000345392.2:c.309_340+19delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG
NM_000551.3:c.309_340+19delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG , LRG_322t1:c.309_340+19delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG
NM_198156.2:c.309_340+19delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG
XM_011534078.1:c.309_340+19delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG
NM_001354723.1:c.309_340+19delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG
NM_000551.4:c.309_340+19delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG
NM_001354723.2:c.309_340+19delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG
NM_198156.3:c.309_340+19delinsTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAG