Canonical Allele Identifier: CA645525015
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs1131690954
COSMIC: COSM17774

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10146639A>T , CM000665.2:g.10146639A>T GRCh38
NC_000003.11:g.10188323A>T , CM000665.1:g.10188323A>T GRCh37
NC_000003.10:g.10163323A>T NCBI36
NG_008212.3:g.10005A>T , LRG_322:g.10005A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*140+3A>T ENSP00000512434.1:n.*140+3A>T
ENST00000696143.1:c.600-3148A>T ENSP00000512435.1:n.600-3148A>T
ENST00000696153.1:c.463+3A>T ENSP00000512444.1:n.463+3A>T
ENST00000256474.3:c.463+3A>T MANE Select ENSP00000256474.3:n.463+3A>T
ENST00000256474.2:c.463+3A>T ENSP00000256474.2:n.463+3A>T
ENST00000345392.2:c.341-3148A>T ENSP00000344757.2:n.341-3148A>T
ENST00000477538.1:n.599+3A>T
NM_000551.3:c.463+3A>T , LRG_322t1:c.463+3A>T NP_000542.1:n.463+3A>T
NM_198156.2:c.341-3148A>T NP_937799.1:n.341-3148A>T
NM_001354723.1:c.*18-3148A>T NP_001341652.1:n.*18-3148A>T
NM_000551.4:c.463+3A>T MANE Select NP_000542.1:n.463+3A>T
NM_001354723.2:c.*18-3148A>T NP_001341652.1:n.*18-3148A>T
NM_198156.3:c.341-3148A>T NP_937799.1:n.341-3148A>T