Canonical Allele Identifier: CA357072
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223176
dbSNP Id: rs864321643
COSMIC: COSM144973
CIViC: CA357072

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10142140A>G , CM000665.2:g.10142140A>G GRCh38
NC_000003.11:g.10183824A>G , CM000665.1:g.10183824A>G GRCh37
NC_000003.10:g.10158824A>G NCBI36
NG_008212.3:g.5506A>G , LRG_322:g.5506A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.293A>G ENSP00000512434.1:p.Tyr98Cys
ENST00000696143.1:c.293A>G ENSP00000512435.1:p.Tyr98Cys
ENST00000696153.1:c.293A>G ENSP00000512444.1:p.Tyr98Cys
ENST00000256474.3:c.293A>G MANE Select ENSP00000256474.3:p.Tyr98Cys
ENST00000256474.2:c.293A>G ENSP00000256474.2:p.Tyr98Cys
ENST00000345392.2:c.293A>G ENSP00000344757.2:p.Tyr98Cys
NM_000551.3:c.293A>G , LRG_322t1:c.293A>G NP_000542.1:p.Tyr98Cys
NM_198156.2:c.293A>G NP_937799.1:p.Tyr98Cys
XM_011534078.1:c.293A>G XP_011532380.1:p.Tyr98Cys
NM_001354723.1:c.293A>G NP_001341652.1:p.Tyr98Cys
NM_000551.4:c.293A>G MANE Select NP_000542.1:p.Tyr98Cys
NM_001354723.2:c.293A>G NP_001341652.1:p.Tyr98Cys
NM_198156.3:c.293A>G NP_937799.1:p.Tyr98Cys