Canonical Allele Identifier: CA1345058639
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10146578A= , CM000665.2:g.10146578A= GRCh38
NC_000003.11:g.10188262A= , CM000665.1:g.10188262A= GRCh37
NC_000003.10:g.10163262A= NCBI36
NG_008212.3:g.9944A= , LRG_322:g.9944A=

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*82A= ENSP00000512434.1:n.*82A=
ENST00000696143.1:c.600-3209A= ENSP00000512435.1:n.600-3209A=
ENST00000696153.1:c.405A= ENSP00000512444.1:p.Leu135=
ENST00000256474.3:c.405A= MANE Select ENSP00000256474.3:p.Leu135=
ENST00000256474.2:c.405A= ENSP00000256474.2:p.Leu135=
ENST00000345392.2:c.341-3209A= ENSP00000344757.2:n.341-3209A=
ENST00000477538.1:n.541A=
NM_000551.3:c.405A= , LRG_322t1:c.405A= NP_000542.1:p.Leu135=
NM_198156.2:c.341-3209A= NP_937799.1:n.341-3209A=
XM_011534078.1:c.*82A= XP_011532380.1:n.*82A=
NM_001354723.1:c.*18-3209A= NP_001341652.1:n.*18-3209A=
NM_000551.4:c.405A= MANE Select NP_000542.1:p.Leu135=
NM_001354723.2:c.*18-3209A= NP_001341652.1:n.*18-3209A=
NM_198156.3:c.341-3209A= NP_937799.1:n.341-3209A=