Canonical Allele Identifier: CA1139655746
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 934978
ClinVar RCV Id: RCV001203476
dbSNP Id: rs1241756327
gnomAD v4: 3-10142976-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10142976C>T , CM000665.2:g.10142976C>T GRCh38
NC_000003.11:g.10184660C>T , CM000665.1:g.10184660C>T GRCh37
NC_000003.10:g.10159660C>T NCBI36
NG_008212.3:g.6342C>T , LRG_322:g.6342C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.554C>T ENSP00000512434.1:p.Pro185Leu
ENST00000696143.1:c.554C>T ENSP00000512435.1:p.Pro185Leu
ENST00000696153.1:c.340+789C>T ENSP00000512444.1:n.340+789C>T
ENST00000256474.3:c.340+789C>T MANE Select ENSP00000256474.3:n.340+789C>T
ENST00000256474.2:c.340+789C>T ENSP00000256474.2:n.340+789C>T
ENST00000345392.2:c.340+789C>T ENSP00000344757.2:n.340+789C>T
ENST00000477538.1:n.431C>T
NM_000551.3:c.340+789C>T , LRG_322t1:c.340+789C>T NP_000542.1:n.340+789C>T
NM_198156.2:c.340+789C>T NP_937799.1:n.340+789C>T
XM_011534078.1:c.554C>T XP_011532380.1:p.Pro185Leu
NM_001354723.1:c.554C>T NP_001341652.1:p.Pro185Leu
NM_000551.4:c.340+789C>T MANE Select NP_000542.1:n.340+789C>T
NM_001354723.2:c.554C>T NP_001341652.1:p.Pro185Leu
NM_198156.3:c.340+789C>T NP_937799.1:n.340+789C>T