Canonical Allele Identifier: CA432423146
Gene: VHL HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.10191488C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149804C>A , CM000665.2:g.10149804C>A GRCh38
NC_000003.11:g.10191488C>A , CM000665.1:g.10191488C>A GRCh37
NC_000003.10:g.10166488C>A NCBI36
NG_008212.3:g.13170C>A , LRG_322:g.13170C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*158C>A ENSP00000512434.1:n.*158C>A
ENST00000696143.1:c.617C>A ENSP00000512435.1:n.617C>A
ENST00000696153.1:c.592C>A ENSP00000512444.1:p.Arg198=
ENST00000256474.3:c.481C>A MANE Select ENSP00000256474.3:p.Arg161=
ENST00000256474.2:c.481C>A ENSP00000256474.2:p.Arg161=
ENST00000345392.2:c.358C>A ENSP00000344757.2:p.Arg120=
ENST00000477538.1:n.617C>A
NM_000551.3:c.481C>A , LRG_322t1:c.481C>A NP_000542.1:p.Arg161=
NM_198156.2:c.358C>A NP_937799.1:p.Arg120=
NM_001354723.1:c.*35C>A NP_001341652.1:n.*35C>A
NM_000551.4:c.481C>A MANE Select NP_000542.1:p.Arg161=
NM_001354723.2:c.*35C>A NP_001341652.1:n.*35C>A
NM_198156.3:c.358C>A NP_937799.1:p.Arg120=