Canonical Allele Identifier: CA351756545
Gene: VHL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149916T>G , CM000665.2:g.10149916T>G GRCh38
NC_000003.11:g.10191600T>G , CM000665.1:g.10191600T>G GRCh37
NC_000003.10:g.10166600T>G NCBI36
NG_008212.3:g.13282T>G , LRG_322:g.13282T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*270T>G ENSP00000512434.1:n.*270T>G
ENST00000696143.1:c.729T>G ENSP00000512435.1:n.729T>G
ENST00000696153.1:c.704T>G ENSP00000512444.1:p.Leu235Arg
ENST00000256474.3:c.593T>G MANE Select ENSP00000256474.3:p.Leu198Arg
ENST00000256474.2:c.593T>G ENSP00000256474.2:p.Leu198Arg
ENST00000345392.2:c.470T>G ENSP00000344757.2:p.Leu157Arg
ENST00000477538.1:n.729T>G
NM_000551.3:c.593T>G , LRG_322t1:c.593T>G NP_000542.1:p.Leu198Arg
NM_198156.2:c.470T>G NP_937799.1:p.Leu157Arg
NM_001354723.1:c.*147T>G NP_001341652.1:n.*147T>G
NM_000551.4:c.593T>G MANE Select NP_000542.1:p.Leu198Arg
NM_001354723.2:c.*147T>G NP_001341652.1:n.*147T>G
NM_198156.3:c.470T>G NP_937799.1:p.Leu157Arg