Canonical Allele Identifier: CA645525027
Gene: VHL HGNC NCBI

Linked Data

COSMIC: COSM30326

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149786_10149794del , CM000665.2:g.10149786_10149794del GRCh38
NC_000003.11:g.10191470_10191478del , CM000665.1:g.10191470_10191478del GRCh37
NC_000003.10:g.10166470_10166478del NCBI36
NG_008212.3:g.13152_13160del , LRG_322:g.13152_13160del

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*141-1_*148del
ENST00000696143.1:c.600-1_607del
ENST00000696153.1:c.575-1_582del
ENST00000256474.3:c.464-1_471del
ENST00000256474.2:c.464-1_471del
ENST00000345392.2:c.341-1_348del
ENST00000477538.1:n.600-1_607del
NM_000551.3:c.464-1_471del , LRG_322t1:c.464-1_471del
NM_198156.2:c.341-1_348del
NM_001354723.1:c.*18-1_*25del
NM_000551.4:c.464-1_471del
NM_001354723.2:c.*18-1_*25del
NM_198156.3:c.341-1_348del