Canonical Allele Identifier: CA1345068950
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10145062T= , CM000665.2:g.10145062T= GRCh38
NC_000003.11:g.10186746T= , CM000665.1:g.10186746T= GRCh37
NC_000003.10:g.10161746T= NCBI36
NG_008212.3:g.8428T= , LRG_322:g.8428T=

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*18-1452T= ENSP00000512434.1:n.*18-1452T=
ENST00000696143.1:c.599+2041T= ENSP00000512435.1:n.599+2041T=
ENST00000696153.1:c.341-1452T= ENSP00000512444.1:n.341-1452T=
ENST00000256474.3:c.341-1452T= MANE Select ENSP00000256474.3:n.341-1452T=
ENST00000256474.2:c.341-1452T= ENSP00000256474.2:n.341-1452T=
ENST00000345392.2:c.340+2875T= ENSP00000344757.2:n.340+2875T=
ENST00000477538.1:n.477-1452T=
NM_000551.3:c.341-1452T= , LRG_322t1:c.341-1452T= NP_000542.1:n.341-1452T=
NM_198156.2:c.340+2875T= NP_937799.1:n.340+2875T=
XM_011534078.1:c.*18-1452T= XP_011532380.1:n.*18-1452T=
NM_001354723.1:c.*17+2041T= NP_001341652.1:n.*17+2041T=
NM_000551.4:c.341-1452T= MANE Select NP_000542.1:n.341-1452T=
NM_001354723.2:c.*17+2041T= NP_001341652.1:n.*17+2041T=
NM_198156.3:c.340+2875T= NP_937799.1:n.340+2875T=