Canonical Allele Identifier: CA645525069
Gene: VHL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149817_10149818dup , CM000665.2:g.10149817_10149818dup GRCh38
NC_000003.11:g.10191501_10191502dup , CM000665.1:g.10191501_10191502dup GRCh37
NC_000003.10:g.10166501_10166502dup NCBI36
NG_008212.3:g.13183_13184dup , LRG_322:g.13183_13184dup

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*171_*172dup ENSP00000512434.1:n.*171_*172dup
ENST00000696143.1:c.630_631dup ENSP00000512435.1:n.630_631dup
ENST00000696153.1:c.605_606dup ENSP00000512444.1:p.Val203LeufsTer5
ENST00000256474.3:c.494_495dup MANE Select ENSP00000256474.3:p.Val166LeufsTer5
ENST00000256474.2:c.494_495dup ENSP00000256474.2:p.Val166LeufsTer5
ENST00000345392.2:c.371_372dup ENSP00000344757.2:p.Val125LeufsTer5
ENST00000477538.1:n.630_631dup
NM_000551.3:c.494_495dup , LRG_322t1:c.494_495dup NP_000542.1:p.Val166LeufsTer5
NM_198156.2:c.371_372dup NP_937799.1:p.Val125LeufsTer5
NM_001354723.1:c.*48_*49dup NP_001341652.1:n.*48_*49dup
NM_000551.4:c.494_495dup MANE Select NP_000542.1:p.Val166LeufsTer5
NM_001354723.2:c.*48_*49dup NP_001341652.1:n.*48_*49dup
NM_198156.3:c.371_372dup NP_937799.1:p.Val125LeufsTer5