Canonical Allele Identifier: CA351756193
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs1553620326

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149831G>T , CM000665.2:g.10149831G>T GRCh38
NC_000003.11:g.10191515G>T , CM000665.1:g.10191515G>T GRCh37
NC_000003.10:g.10166515G>T NCBI36
NG_008212.3:g.13197G>T , LRG_322:g.13197G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*185G>T ENSP00000512434.1:n.*185G>T
ENST00000696143.1:c.644G>T ENSP00000512435.1:n.644G>T
ENST00000696153.1:c.619G>T ENSP00000512444.1:p.Val207Phe
ENST00000256474.3:c.508G>T MANE Select ENSP00000256474.3:p.Val170Phe
ENST00000256474.2:c.508G>T ENSP00000256474.2:p.Val170Phe
ENST00000345392.2:c.385G>T ENSP00000344757.2:p.Val129Phe
ENST00000477538.1:n.644G>T
NM_000551.3:c.508G>T , LRG_322t1:c.508G>T NP_000542.1:p.Val170Phe
NM_198156.2:c.385G>T NP_937799.1:p.Val129Phe
NM_001354723.1:c.*62G>T NP_001341652.1:n.*62G>T
NM_000551.4:c.508G>T MANE Select NP_000542.1:p.Val170Phe
NM_001354723.2:c.*62G>T NP_001341652.1:n.*62G>T
NM_198156.3:c.385G>T NP_937799.1:p.Val129Phe