Canonical Allele Identifier: CA432423066
Gene: VHL HGNC NCBI

Linked Data

COSMIC: COSM14391
MyVariant Identifiers: chr3:g.10191476del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149792del , CM000665.2:g.10149792del GRCh38
NC_000003.11:g.10191476del , CM000665.1:g.10191476del GRCh37
NC_000003.10:g.10166476del NCBI36
NG_008212.3:g.13158del , LRG_322:g.13158del

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*146del ENSP00000512434.1:n.*146del
ENST00000696143.1:c.605del ENSP00000512435.1:n.605del
ENST00000696153.1:c.580del ENSP00000512444.1:p.Thr194LeufsTer2
ENST00000256474.3:c.469del MANE Select ENSP00000256474.3:p.Thr157LeufsTer2
ENST00000256474.2:c.469del ENSP00000256474.2:p.Thr157LeufsTer2
ENST00000345392.2:c.346del ENSP00000344757.2:p.Thr116LeufsTer2
ENST00000477538.1:n.605del
NM_000551.3:c.469del , LRG_322t1:c.469del NP_000542.1:p.Thr157LeufsTer2
NM_198156.2:c.346del NP_937799.1:p.Thr116LeufsTer2
NM_001354723.1:c.*23del NP_001341652.1:n.*23del
NM_000551.4:c.469del MANE Select NP_000542.1:p.Thr157LeufsTer2
NM_001354723.2:c.*23del NP_001341652.1:n.*23del
NM_198156.3:c.346del NP_937799.1:p.Thr116LeufsTer2