Canonical Allele Identifier: CA645524973
Gene: VHL HGNC NCBI

Linked Data

COSMIC: COSM18133

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10146603_10146606del , CM000665.2:g.10146603_10146606del GRCh38
NC_000003.11:g.10188287_10188290del , CM000665.1:g.10188287_10188290del GRCh37
NC_000003.10:g.10163287_10163290del NCBI36
NG_008212.3:g.9969_9972del , LRG_322:g.9969_9972del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.*107_*110del ENSP00000512434.1:n.*107_*110del
ENST00000696143.1:c.600-3184_600-3181del ENSP00000512435.1:n.600-3184_600-3181del
ENST00000696153.1:c.430_433del ENSP00000512444.1:p.Gly144SerfsTer24
ENST00000256474.3:c.430_433del MANE Select ENSP00000256474.3:p.Gly144SerfsTer14
ENST00000256474.2:c.430_433del ENSP00000256474.2:p.Gly144SerfsTer14
ENST00000345392.2:c.341-3184_341-3181del ENSP00000344757.2:n.341-3184_341-3181del
ENST00000477538.1:n.566_569del
NM_000551.3:c.430_433del , LRG_322t1:c.430_433del NP_000542.1:p.Gly144SerfsTer14
NM_198156.2:c.341-3184_341-3181del NP_937799.1:n.341-3184_341-3181del
NM_001354723.1:c.*18-3184_*18-3181del NP_001341652.1:n.*18-3184_*18-3181del
NM_000551.4:c.430_433del MANE Select NP_000542.1:p.Gly144SerfsTer14
NM_001354723.2:c.*18-3184_*18-3181del NP_001341652.1:n.*18-3184_*18-3181del
NM_198156.3:c.341-3184_341-3181del NP_937799.1:n.341-3184_341-3181del