Canonical Allele Identifier: CA645524811
Gene: VHL HGNC NCBI

Linked Data

COSMIC: COSM30485

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10142131_10142132insA , CM000665.2:g.10142131_10142132insA GRCh38
NC_000003.11:g.10183815_10183816insA , CM000665.1:g.10183815_10183816insA GRCh37
NC_000003.10:g.10158815_10158816insA NCBI36
NG_008212.3:g.5497_5498insA , LRG_322:g.5497_5498insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.284_285insA ENSP00000512434.1:p.Gln96AlafsTer?
ENST00000696143.1:c.284_285insA ENSP00000512435.1:p.Gln96AlafsTer?
ENST00000696153.1:c.284_285insA ENSP00000512444.1:p.Gln96AlafsTer?
ENST00000256474.3:c.284_285insA MANE Select ENSP00000256474.3:p.Gln96AlafsTer?
ENST00000256474.2:c.284_285insA ENSP00000256474.2:p.Gln96AlafsTer?
ENST00000345392.2:c.284_285insA ENSP00000344757.2:p.Gln96AlafsTer?
NM_000551.3:c.284_285insA , LRG_322t1:c.284_285insA NP_000542.1:p.Gln96AlafsTer?
NM_198156.2:c.284_285insA NP_937799.1:p.Gln96AlafsTer?
XM_011534078.1:c.284_285insA XP_011532380.1:p.Gln96AlafsTer?
NM_001354723.1:c.284_285insA NP_001341652.1:p.Gln96AlafsTer?
NM_000551.4:c.284_285insA MANE Select NP_000542.1:p.Gln96AlafsTer?
NM_001354723.2:c.284_285insA NP_001341652.1:p.Gln96AlafsTer?
NM_198156.3:c.284_285insA NP_937799.1:p.Gln96AlafsTer?