Canonical Allele Identifier: CA645525052
Gene: VHL HGNC NCBI

Linked Data

COSMIC: COSM99116

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149802_10149803dup , CM000665.2:g.10149802_10149803dup GRCh38
NC_000003.11:g.10191486_10191487dup , CM000665.1:g.10191486_10191487dup GRCh37
NC_000003.10:g.10166486_10166487dup NCBI36
NG_008212.3:g.13168_13169dup , LRG_322:g.13168_13169dup

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*156_*157dup ENSP00000512434.1:n.*156_*157dup
ENST00000696143.1:c.615_616dup ENSP00000512435.1:n.615_616dup
ENST00000696153.1:c.590_591dup ENSP00000512444.1:p.Arg198SerfsTer10
ENST00000256474.3:c.479_480dup MANE Select ENSP00000256474.3:p.Arg161SerfsTer10
ENST00000256474.2:c.479_480dup ENSP00000256474.2:p.Arg161SerfsTer10
ENST00000345392.2:c.356_357dup ENSP00000344757.2:p.Arg120SerfsTer10
ENST00000477538.1:n.615_616dup
NM_000551.3:c.479_480dup , LRG_322t1:c.479_480dup NP_000542.1:p.Arg161SerfsTer10
NM_198156.2:c.356_357dup NP_937799.1:p.Arg120SerfsTer10
NM_001354723.1:c.*33_*34dup NP_001341652.1:n.*33_*34dup
NM_000551.4:c.479_480dup MANE Select NP_000542.1:p.Arg161SerfsTer10
NM_001354723.2:c.*33_*34dup NP_001341652.1:n.*33_*34dup
NM_198156.3:c.356_357dup NP_937799.1:p.Arg120SerfsTer10