Canonical Allele Identifier: CA645524876
Gene: VHL HGNC NCBI

Linked Data

COSMIC: COSM17643

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10146515_10146524del , CM000665.2:g.10146515_10146524del GRCh38
NC_000003.11:g.10188199_10188208del , CM000665.1:g.10188199_10188208del GRCh37
NC_000003.10:g.10163199_10163208del NCBI36
NG_008212.3:g.9881_9890del , LRG_322:g.9881_9890del

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*19_*28del
ENST00000696143.1:c.600-3272_600-3263del ENSP00000512435.1:n.600-3272_600-3263del
ENST00000696153.1:c.342_351del
ENST00000256474.3:c.342_351del
ENST00000256474.2:c.342_351del
ENST00000345392.2:c.341-3272_341-3263del ENSP00000344757.2:n.341-3272_341-3263del
ENST00000477538.1:n.478_487del
NM_000551.3:c.342_351del , LRG_322t1:c.342_351del
NM_198156.2:c.341-3272_341-3263del NP_937799.1:n.341-3272_341-3263del
XM_011534078.1:c.*19_*28del
NM_001354723.1:c.*18-3272_*18-3263del NP_001341652.1:n.*18-3272_*18-3263del
NM_000551.4:c.342_351del
NM_001354723.2:c.*18-3272_*18-3263del NP_001341652.1:n.*18-3272_*18-3263del
NM_198156.3:c.341-3272_341-3263del NP_937799.1:n.341-3272_341-3263del