Canonical Allele Identifier: CA1345068948
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10145061A= , CM000665.2:g.10145061A= GRCh38
NC_000003.11:g.10186745A= , CM000665.1:g.10186745A= GRCh37
NC_000003.10:g.10161745A= NCBI36
NG_008212.3:g.8427A= , LRG_322:g.8427A=

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*18-1453A= ENSP00000512434.1:n.*18-1453A=
ENST00000696143.1:c.599+2040A= ENSP00000512435.1:n.599+2040A=
ENST00000696153.1:c.341-1453A= ENSP00000512444.1:n.341-1453A=
ENST00000256474.3:c.341-1453A= MANE Select ENSP00000256474.3:n.341-1453A=
ENST00000256474.2:c.341-1453A= ENSP00000256474.2:n.341-1453A=
ENST00000345392.2:c.340+2874A= ENSP00000344757.2:n.340+2874A=
ENST00000477538.1:n.477-1453A=
NM_000551.3:c.341-1453A= , LRG_322t1:c.341-1453A= NP_000542.1:n.341-1453A=
NM_198156.2:c.340+2874A= NP_937799.1:n.340+2874A=
XM_011534078.1:c.*18-1453A= XP_011532380.1:n.*18-1453A=
NM_001354723.1:c.*17+2040A= NP_001341652.1:n.*17+2040A=
NM_000551.4:c.341-1453A= MANE Select NP_000542.1:n.341-1453A=
NM_001354723.2:c.*17+2040A= NP_001341652.1:n.*17+2040A=
NM_198156.3:c.340+2874A= NP_937799.1:n.340+2874A=