Canonical Allele Identifier: CA645529572
Gene: VHL HGNC NCBI

Linked Data

COSMIC: COSM25696

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149910_10149911del , CM000665.2:g.10149910_10149911del GRCh38
NC_000003.11:g.10191594_10191595del , CM000665.1:g.10191594_10191595del GRCh37
NC_000003.10:g.10166594_10166595del NCBI36
NG_008212.3:g.13276_13277del , LRG_322:g.13276_13277del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.*264_*265del ENSP00000512434.1:n.*264_*265del
ENST00000696143.1:c.723_724del ENSP00000512435.1:n.723_724del
ENST00000696153.1:c.698_699del ENSP00000512444.1:p.Lys233ArgfsTer?
ENST00000256474.3:c.587_588del MANE Select ENSP00000256474.3:p.Lys196ArgfsTer?
ENST00000256474.2:c.587_588del ENSP00000256474.2:p.Lys196ArgfsTer?
ENST00000345392.2:c.464_465del ENSP00000344757.2:p.Lys155ArgfsTer?
ENST00000477538.1:n.723_724del
NM_000551.3:c.587_588del , LRG_322t1:c.587_588del NP_000542.1:p.Lys196ArgfsTer?
NM_198156.2:c.464_465del NP_937799.1:p.Lys155ArgfsTer?
NM_001354723.1:c.*141_*142del NP_001341652.1:n.*141_*142del
NM_000551.4:c.587_588del MANE Select NP_000542.1:p.Lys196ArgfsTer?
NM_001354723.2:c.*141_*142del NP_001341652.1:n.*141_*142del
NM_198156.3:c.464_465del NP_937799.1:p.Lys155ArgfsTer?