Canonical Allele Identifier: CA645525089
Gene: VHL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149839del , CM000665.2:g.10149839del GRCh38
NC_000003.11:g.10191523del , CM000665.1:g.10191523del GRCh37
NC_000003.10:g.10166523del NCBI36
NG_008212.3:g.13205del , LRG_322:g.13205del

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*193del ENSP00000512434.1:n.*193del
ENST00000696143.1:c.652del ENSP00000512435.1:n.652del
ENST00000696153.1:c.627del ENSP00000512444.1:p.Glu210ArgfsTer29
ENST00000256474.3:c.516del MANE Select ENSP00000256474.3:p.Glu173ArgfsTer29
ENST00000256474.2:c.516del ENSP00000256474.2:p.Glu173ArgfsTer29
ENST00000345392.2:c.393del ENSP00000344757.2:p.Glu132ArgfsTer29
ENST00000477538.1:n.652del
NM_000551.3:c.516del , LRG_322t1:c.516del NP_000542.1:p.Glu173ArgfsTer29
NM_198156.2:c.393del NP_937799.1:p.Glu132ArgfsTer29
NM_001354723.1:c.*70del NP_001341652.1:n.*70del
NM_000551.4:c.516del MANE Select NP_000542.1:p.Glu173ArgfsTer29
NM_001354723.2:c.*70del NP_001341652.1:n.*70del
NM_198156.3:c.393del NP_937799.1:p.Glu132ArgfsTer29