Canonical Allele Identifier: CA645529568
Gene: VHL HGNC NCBI

Linked Data

COSMIC: COSM17921

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149901dup , CM000665.2:g.10149901dup GRCh38
NC_000003.11:g.10191585dup , CM000665.1:g.10191585dup GRCh37
NC_000003.10:g.10166585dup NCBI36
NG_008212.3:g.13267dup , LRG_322:g.13267dup

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*255dup ENSP00000512434.1:n.*255dup
ENST00000696143.1:c.714dup ENSP00000512435.1:n.714dup
ENST00000696153.1:c.689dup ENSP00000512444.1:p.Asn230LysfsTer?
ENST00000256474.3:c.578dup MANE Select ENSP00000256474.3:p.Asn193LysfsTer?
ENST00000256474.2:c.578dup ENSP00000256474.2:p.Asn193LysfsTer?
ENST00000345392.2:c.455dup ENSP00000344757.2:p.Asn152LysfsTer?
ENST00000477538.1:n.714dup
NM_000551.3:c.578dup , LRG_322t1:c.578dup NP_000542.1:p.Asn193LysfsTer?
NM_198156.2:c.455dup NP_937799.1:p.Asn152LysfsTer?
NM_001354723.1:c.*132dup NP_001341652.1:n.*132dup
NM_000551.4:c.578dup MANE Select NP_000542.1:p.Asn193LysfsTer?
NM_001354723.2:c.*132dup NP_001341652.1:n.*132dup
NM_198156.3:c.455dup NP_937799.1:p.Asn152LysfsTer?