Canonical Allele Identifier: CA1345059771
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10147579G= , CM000665.2:g.10147579G= GRCh38
NC_000003.11:g.10189263G= , CM000665.1:g.10189263G= GRCh37
NC_000003.10:g.10164263G= NCBI36
NG_008212.3:g.10945G= , LRG_322:g.10945G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*140+943G= ENSP00000512434.1:n.*140+943G=
ENST00000696143.1:c.600-2208G= ENSP00000512435.1:n.600-2208G=
ENST00000696153.1:c.463+943G= ENSP00000512444.1:n.463+943G=
ENST00000256474.3:c.463+943G= MANE Select ENSP00000256474.3:n.463+943G=
ENST00000256474.2:c.463+943G= ENSP00000256474.2:n.463+943G=
ENST00000345392.2:c.341-2208G= ENSP00000344757.2:n.341-2208G=
ENST00000477538.1:n.599+943G=
NM_000551.3:c.463+943G= , LRG_322t1:c.463+943G= NP_000542.1:n.463+943G=
NM_198156.2:c.341-2208G= NP_937799.1:n.341-2208G=
NM_001354723.1:c.*18-2208G= NP_001341652.1:n.*18-2208G=
NM_000551.4:c.463+943G= MANE Select NP_000542.1:n.463+943G=
NM_001354723.2:c.*18-2208G= NP_001341652.1:n.*18-2208G=
NM_198156.3:c.341-2208G= NP_937799.1:n.341-2208G=