Canonical Allele Identifier: CA645525084
Gene: VHL HGNC NCBI

Linked Data

COSMIC: COSM26794

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149837_10149850del , CM000665.2:g.10149837_10149850del GRCh38
NC_000003.11:g.10191521_10191534del , CM000665.1:g.10191521_10191534del GRCh37
NC_000003.10:g.10166521_10166534del NCBI36
NG_008212.3:g.13203_13216del , LRG_322:g.13203_13216del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.*191_*204del ENSP00000512434.1:n.*191_*204del
ENST00000696143.1:c.650_663del ENSP00000512435.1:n.650_663del
ENST00000696153.1:c.625_638del ENSP00000512444.1:p.Pro209GlufsTer?
ENST00000256474.3:c.514_527del MANE Select ENSP00000256474.3:p.Pro172GlufsTer?
ENST00000256474.2:c.514_527del ENSP00000256474.2:p.Pro172GlufsTer?
ENST00000345392.2:c.391_404del ENSP00000344757.2:p.Pro131GlufsTer?
ENST00000477538.1:n.650_663del
NM_000551.3:c.514_527del , LRG_322t1:c.514_527del NP_000542.1:p.Pro172GlufsTer?
NM_198156.2:c.391_404del NP_937799.1:p.Pro131GlufsTer?
NM_001354723.1:c.*68_*81del NP_001341652.1:n.*68_*81del
NM_000551.4:c.514_527del MANE Select NP_000542.1:p.Pro172GlufsTer?
NM_001354723.2:c.*68_*81del NP_001341652.1:n.*68_*81del
NM_198156.3:c.391_404del NP_937799.1:p.Pro131GlufsTer?