Canonical Allele Identifier: CA2573136120

Gene: VHL

Linked Data

• ClinVar Variation Id: 1441653
• ClinVar RCV Id: RCV001950691
• dbSNP Id: rs2125125997

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142889_10142892del , CM000665.2:g.10142889_10142892del	GRCh38
NC_000003.11:g.10184573_10184576del , CM000665.1:g.10184573_10184576del	GRCh37
NC_000003.10:g.10159573_10159576del	NCBI36
NG_008212.3:g.6255_6258del , LRG_322:g.6255_6258del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.467_470del	ENSP00000512434.1:p.Asp156ValfsTer7
ENST00000696143.1:c.467_470del	ENSP00000512435.1:p.Asp156ValfsTer7
ENST00000696153.1:c.340+702_340+705del	ENSP00000512444.1:n.340+702_340+705del
ENST00000256474.3:c.340+702_340+705del MANE Select	ENSP00000256474.3:n.340+702_340+705del
ENST00000256474.2:c.340+702_340+705del	ENSP00000256474.2:n.340+702_340+705del
ENST00000345392.2:c.340+702_340+705del	ENSP00000344757.2:n.340+702_340+705del
ENST00000477538.1:n.344_347del
NM_000551.3:c.340+702_340+705del , LRG_322t1:c.340+702_340+705del	NP_000542.1:n.340+702_340+705del
NM_198156.2:c.340+702_340+705del	NP_937799.1:n.340+702_340+705del
XM_011534078.1:c.467_470del	XP_011532380.1:p.Asp156ValfsTer7
NM_001354723.1:c.467_470del	NP_001341652.1:p.Asp156ValfsTer7
NM_000551.4:c.340+702_340+705del MANE Select	NP_000542.1:n.340+702_340+705del
NM_001354723.2:c.467_470del	NP_001341652.1:p.Asp156ValfsTer7
NM_198156.3:c.340+702_340+705del	NP_937799.1:n.340+702_340+705del