Canonical Allele Identifier: CA645525029
Gene: VHL HGNC NCBI

Linked Data

COSMIC: COSM17979

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149787_10149797del , CM000665.2:g.10149787_10149797del GRCh38
NC_000003.11:g.10191471_10191481del , CM000665.1:g.10191471_10191481del GRCh37
NC_000003.10:g.10166471_10166481del NCBI36
NG_008212.3:g.13153_13163del , LRG_322:g.13153_13163del

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*141_*151del
ENST00000696143.1:c.600_610del
ENST00000696153.1:c.575_585del
ENST00000256474.3:c.464_474del
ENST00000256474.2:c.464_474del
ENST00000345392.2:c.341_351del
ENST00000477538.1:n.600_610del
NM_000551.3:c.464_474del , LRG_322t1:c.464_474del
NM_198156.2:c.341_351del
NM_001354723.1:c.*18_*28del
NM_000551.4:c.464_474del
NM_001354723.2:c.*18_*28del
NM_198156.3:c.341_351del