Canonical Allele Identifier: CA645524715
Gene: VHL HGNC NCBI

Linked Data

COSMIC: COSM17682

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10142068_10142077del , CM000665.2:g.10142068_10142077del GRCh38
NC_000003.11:g.10183752_10183761del , CM000665.1:g.10183752_10183761del GRCh37
NC_000003.10:g.10158752_10158761del NCBI36
NG_008212.3:g.5434_5443del , LRG_322:g.5434_5443del

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.221_230del ENSP00000512434.1:p.Val74AlafsTer?
ENST00000696143.1:c.221_230del ENSP00000512435.1:p.Val74AlafsTer?
ENST00000696153.1:c.221_230del ENSP00000512444.1:p.Val74AlafsTer?
ENST00000256474.3:c.221_230del MANE Select ENSP00000256474.3:p.Val74AlafsTer?
ENST00000256474.2:c.221_230del ENSP00000256474.2:p.Val74AlafsTer?
ENST00000345392.2:c.221_230del ENSP00000344757.2:p.Val74AlafsTer?
NM_000551.3:c.221_230del , LRG_322t1:c.221_230del NP_000542.1:p.Val74AlafsTer?
NM_198156.2:c.221_230del NP_937799.1:p.Val74AlafsTer?
XM_011534078.1:c.221_230del XP_011532380.1:p.Val74AlafsTer?
NM_001354723.1:c.221_230del NP_001341652.1:p.Val74AlafsTer?
NM_000551.4:c.221_230del MANE Select NP_000542.1:p.Val74AlafsTer?
NM_001354723.2:c.221_230del NP_001341652.1:p.Val74AlafsTer?
NM_198156.3:c.221_230del NP_937799.1:p.Val74AlafsTer?