Canonical Allele Identifier: CA1345063552
Gene: VHL HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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