Canonical Allele Identifier: CA432421803
Gene: VHL HGNC NCBI

Linked Data

COSMIC: COSM423192
MyVariant Identifiers: chr3:g.10188218del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10146534del , CM000665.2:g.10146534del GRCh38
NC_000003.11:g.10188218del , CM000665.1:g.10188218del GRCh37
NC_000003.10:g.10163218del NCBI36
NG_008212.3:g.9900del , LRG_322:g.9900del

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*38del ENSP00000512434.1:n.*38del
ENST00000696143.1:c.600-3253del ENSP00000512435.1:n.600-3253del
ENST00000696153.1:c.361del ENSP00000512444.1:p.Asp121MetfsTer?
ENST00000256474.3:c.361del MANE Select ENSP00000256474.3:p.Asp121MetfsTer?
ENST00000256474.2:c.361del ENSP00000256474.2:p.Asp121MetfsTer?
ENST00000345392.2:c.341-3253del ENSP00000344757.2:n.341-3253del
ENST00000477538.1:n.497del
NM_000551.3:c.361del , LRG_322t1:c.361del NP_000542.1:p.Asp121MetfsTer?
NM_198156.2:c.341-3253del NP_937799.1:n.341-3253del
XM_011534078.1:c.*38del XP_011532380.1:n.*38del
NM_001354723.1:c.*18-3253del NP_001341652.1:n.*18-3253del
NM_000551.4:c.361del MANE Select NP_000542.1:p.Asp121MetfsTer?
NM_001354723.2:c.*18-3253del NP_001341652.1:n.*18-3253del
NM_198156.3:c.341-3253del NP_937799.1:n.341-3253del