Canonical Allele Identifier: CA645524857
Gene: VHL HGNC NCBI

Linked Data

COSMIC: COSM18288

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10142179_10142188del , CM000665.2:g.10142179_10142188del GRCh38
NC_000003.11:g.10183863_10183872del , CM000665.1:g.10183863_10183872del GRCh37
NC_000003.10:g.10158863_10158872del NCBI36
NG_008212.3:g.5545_5554del , LRG_322:g.5545_5554del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.332_340+1del
ENST00000696143.1:c.332_340+1del
ENST00000696153.1:c.332_340+1del
ENST00000256474.3:c.332_340+1del
ENST00000256474.2:c.332_340+1del
ENST00000345392.2:c.332_340+1del
NM_000551.3:c.332_340+1del , LRG_322t1:c.332_340+1del
NM_198156.2:c.332_340+1del
XM_011534078.1:c.332_340+1del
NM_001354723.1:c.332_340+1del
NM_000551.4:c.332_340+1del
NM_001354723.2:c.332_340+1del
NM_198156.3:c.332_340+1del