Canonical Allele Identifier: CA432421871
Gene: VHL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10146591dup , CM000665.2:g.10146591dup GRCh38
NC_000003.11:g.10188275dup , CM000665.1:g.10188275dup GRCh37
NC_000003.10:g.10163275dup NCBI36
NG_008212.3:g.9957dup , LRG_322:g.9957dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.*95dup ENSP00000512434.1:n.*95dup
ENST00000696143.1:c.600-3196dup ENSP00000512435.1:n.600-3196dup
ENST00000696153.1:c.418dup ENSP00000512444.1:p.Leu140ProfsTer4
ENST00000256474.3:c.418dup MANE Select ENSP00000256474.3:p.Leu140ProfsTer4
ENST00000256474.2:c.418dup ENSP00000256474.2:p.Leu140ProfsTer4
ENST00000345392.2:c.341-3196dup ENSP00000344757.2:n.341-3196dup
ENST00000477538.1:n.554dup
NM_000551.3:c.418dup , LRG_322t1:c.418dup NP_000542.1:p.Leu140ProfsTer4
NM_198156.2:c.341-3196dup NP_937799.1:n.341-3196dup
XM_011534078.1:c.*95dup XP_011532380.1:n.*95dup
NM_001354723.1:c.*18-3196dup NP_001341652.1:n.*18-3196dup
NM_000551.4:c.418dup MANE Select NP_000542.1:p.Leu140ProfsTer4
NM_001354723.2:c.*18-3196dup NP_001341652.1:n.*18-3196dup
NM_198156.3:c.341-3196dup NP_937799.1:n.341-3196dup