Canonical Allele Identifier: CA70052556
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs5030650

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149904_10149905del , CM000665.2:g.10149904_10149905del GRCh38
NC_000003.11:g.10191588_10191589del , CM000665.1:g.10191588_10191589del GRCh37
NC_000003.10:g.10166588_10166589del NCBI36
NG_008212.3:g.13270_13271del , LRG_322:g.13270_13271del

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*258_*259del ENSP00000512434.1:n.*258_*259del
ENST00000696143.1:c.717_718del ENSP00000512435.1:n.717_718del
ENST00000696153.1:c.692_693del ENSP00000512444.1:p.Val231AlafsTer?
ENST00000256474.3:c.581_582del MANE Select ENSP00000256474.3:p.Val194AlafsTer?
ENST00000256474.2:c.581_582del ENSP00000256474.2:p.Val194AlafsTer?
ENST00000345392.2:c.458_459del ENSP00000344757.2:p.Val153AlafsTer?
ENST00000477538.1:n.717_718del
NM_000551.3:c.581_582del , LRG_322t1:c.581_582del NP_000542.1:p.Val194AlafsTer?
NM_198156.2:c.458_459del NP_937799.1:p.Val153AlafsTer?
NM_001354723.1:c.*135_*136del NP_001341652.1:n.*135_*136del
NM_000551.4:c.581_582del MANE Select NP_000542.1:p.Val194AlafsTer?
NM_001354723.2:c.*135_*136del NP_001341652.1:n.*135_*136del
NM_198156.3:c.458_459del NP_937799.1:p.Val153AlafsTer?