Canonical Allele Identifier: CA2664400300
Gene: VHL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10150345del , CM000665.2:g.10150345del GRCh38
NC_000003.11:g.10192029del , CM000665.1:g.10192029del GRCh37
NC_000003.10:g.10167029del NCBI36
NG_008212.3:g.13711del , LRG_322:g.13711del

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*699del ENSP00000512434.1:n.*699del
ENST00000696143.1:c.1158del ENSP00000512435.1:n.1158del
ENST00000696153.1:c.*380del ENSP00000512444.1:n.*380del
ENST00000256474.3:c.*380del MANE Select ENSP00000256474.3:n.*380del
ENST00000256474.2:c.*380del ENSP00000256474.2:n.*380del
ENST00000345392.2:c.*380del ENSP00000344757.2:n.*380del
NM_000551.3:c.*380del , LRG_322t1:c.*380del NP_000542.1:n.*380del
NM_198156.2:c.*380del NP_937799.1:n.*380del
NM_001354723.1:c.*576del NP_001341652.1:n.*576del
NM_000551.4:c.*380del MANE Select NP_000542.1:n.*380del
NM_001354723.2:c.*576del NP_001341652.1:n.*576del
NM_198156.3:c.*380del NP_937799.1:n.*380del