Canonical Allele Identifier: CA645524992
Gene: VHL HGNC NCBI

Linked Data

COSMIC: COSM253376

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10146616_10146617dup , CM000665.2:g.10146616_10146617dup GRCh38
NC_000003.11:g.10188300_10188301dup , CM000665.1:g.10188300_10188301dup GRCh37
NC_000003.10:g.10163300_10163301dup NCBI36
NG_008212.3:g.9982_9983dup , LRG_322:g.9982_9983dup

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*120_*121dup ENSP00000512434.1:n.*120_*121dup
ENST00000696143.1:c.600-3171_600-3170dup ENSP00000512435.1:n.600-3171_600-3170dup
ENST00000696153.1:c.443_444dup ENSP00000512444.1:p.Ala149LeufsTer21
ENST00000256474.3:c.443_444dup MANE Select ENSP00000256474.3:p.Ala149LeufsTer11
ENST00000256474.2:c.443_444dup ENSP00000256474.2:p.Ala149LeufsTer11
ENST00000345392.2:c.341-3171_341-3170dup ENSP00000344757.2:n.341-3171_341-3170dup
ENST00000477538.1:n.579_580dup
NM_000551.3:c.443_444dup , LRG_322t1:c.443_444dup NP_000542.1:p.Ala149LeufsTer11
NM_198156.2:c.341-3171_341-3170dup NP_937799.1:n.341-3171_341-3170dup
NM_001354723.1:c.*18-3171_*18-3170dup NP_001341652.1:n.*18-3171_*18-3170dup
NM_000551.4:c.443_444dup MANE Select NP_000542.1:p.Ala149LeufsTer11
NM_001354723.2:c.*18-3171_*18-3170dup NP_001341652.1:n.*18-3171_*18-3170dup
NM_198156.3:c.341-3171_341-3170dup NP_937799.1:n.341-3171_341-3170dup