Canonical Allele Identifier: CA351756038
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs2125130454

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149789T>A , CM000665.2:g.10149789T>A GRCh38
NC_000003.11:g.10191473T>A , CM000665.1:g.10191473T>A GRCh37
NC_000003.10:g.10166473T>A NCBI36
NG_008212.3:g.13155T>A , LRG_322:g.13155T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*143T>A ENSP00000512434.1:n.*143T>A
ENST00000696143.1:c.602T>A ENSP00000512435.1:n.602T>A
ENST00000696153.1:c.577T>A ENSP00000512444.1:p.Tyr193Asn
ENST00000256474.3:c.466T>A MANE Select ENSP00000256474.3:p.Tyr156Asn
ENST00000256474.2:c.466T>A ENSP00000256474.2:p.Tyr156Asn
ENST00000345392.2:c.343T>A ENSP00000344757.2:p.Tyr115Asn
ENST00000477538.1:n.602T>A
NM_000551.3:c.466T>A , LRG_322t1:c.466T>A NP_000542.1:p.Tyr156Asn
NM_198156.2:c.343T>A NP_937799.1:p.Tyr115Asn
NM_001354723.1:c.*20T>A NP_001341652.1:n.*20T>A
NM_000551.4:c.466T>A MANE Select NP_000542.1:p.Tyr156Asn
NM_001354723.2:c.*20T>A NP_001341652.1:n.*20T>A
NM_198156.3:c.343T>A NP_937799.1:p.Tyr115Asn