Canonical Allele Identifier: CA351756181
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs2125130548

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149825A>T , CM000665.2:g.10149825A>T GRCh38
NC_000003.11:g.10191509A>T , CM000665.1:g.10191509A>T GRCh37
NC_000003.10:g.10166509A>T NCBI36
NG_008212.3:g.13191A>T , LRG_322:g.13191A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*179A>T ENSP00000512434.1:n.*179A>T
ENST00000696143.1:c.638A>T ENSP00000512435.1:n.638A>T
ENST00000696153.1:c.613A>T ENSP00000512444.1:p.Ser205Cys
ENST00000256474.3:c.502A>T MANE Select ENSP00000256474.3:p.Ser168Cys
ENST00000256474.2:c.502A>T ENSP00000256474.2:p.Ser168Cys
ENST00000345392.2:c.379A>T ENSP00000344757.2:p.Ser127Cys
ENST00000477538.1:n.638A>T
NM_000551.3:c.502A>T , LRG_322t1:c.502A>T NP_000542.1:p.Ser168Cys
NM_198156.2:c.379A>T NP_937799.1:p.Ser127Cys
NM_001354723.1:c.*56A>T NP_001341652.1:n.*56A>T
NM_000551.4:c.502A>T MANE Select NP_000542.1:p.Ser168Cys
NM_001354723.2:c.*56A>T NP_001341652.1:n.*56A>T
NM_198156.3:c.379A>T NP_937799.1:p.Ser127Cys