Canonical Allele Identifier: CA1345064483
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141779C= , CM000665.2:g.10141779C= GRCh38
NC_000003.11:g.10183463C= , CM000665.1:g.10183463C= GRCh37
NC_000003.10:g.10158463C= NCBI36
NG_008212.3:g.5145C= , LRG_322:g.5145C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696153.1:c.-69C= ENSP00000512444.1:n.-69C=
ENST00000256474.3:c.-69C= MANE Select ENSP00000256474.3:n.-69C=
ENST00000256474.2:c.-69C= ENSP00000256474.2:n.-69C=
NM_000551.3:c.-69C= , LRG_322t1:c.-69C= NP_000542.1:n.-69C=
NM_198156.2:c.-69C= NP_937799.1:n.-69C=
XM_011534078.1:c.-69C= XP_011532380.1:n.-69C=
NM_001354723.1:c.-69C= NP_001341652.1:n.-69C=
NM_000551.4:c.-69C= MANE Select NP_000542.1:n.-69C=
NM_001354723.2:c.-69C= NP_001341652.1:n.-69C=
NM_198156.3:c.-69C= NP_937799.1:n.-69C=