Canonical Allele Identifier: CA351756228
Gene: VHL HGNC NCBI

Linked Data

COSMIC: COSM17917

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149846T>G , CM000665.2:g.10149846T>G GRCh38
NC_000003.11:g.10191530T>G , CM000665.1:g.10191530T>G GRCh37
NC_000003.10:g.10166530T>G NCBI36
NG_008212.3:g.13212T>G , LRG_322:g.13212T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*200T>G ENSP00000512434.1:n.*200T>G
ENST00000696143.1:c.659T>G ENSP00000512435.1:n.659T>G
ENST00000696153.1:c.634T>G ENSP00000512444.1:p.Tyr212Asp
ENST00000256474.3:c.523T>G MANE Select ENSP00000256474.3:p.Tyr175Asp
ENST00000256474.2:c.523T>G ENSP00000256474.2:p.Tyr175Asp
ENST00000345392.2:c.400T>G ENSP00000344757.2:p.Tyr134Asp
ENST00000477538.1:n.659T>G
NM_000551.3:c.523T>G , LRG_322t1:c.523T>G NP_000542.1:p.Tyr175Asp
NM_198156.2:c.400T>G NP_937799.1:p.Tyr134Asp
NM_001354723.1:c.*77T>G NP_001341652.1:n.*77T>G
NM_000551.4:c.523T>G MANE Select NP_000542.1:p.Tyr175Asp
NM_001354723.2:c.*77T>G NP_001341652.1:n.*77T>G
NM_198156.3:c.400T>G NP_937799.1:p.Tyr134Asp