Canonical Allele Identifier: CA2573136130

Gene: VHL

Linked Data

• ClinVar Variation Id: 1418580
• ClinVar RCV Id: RCV001930979
• dbSNP Id: rs2125126052

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142933dup , CM000665.2:g.10142933dup	GRCh38
NC_000003.11:g.10184617dup , CM000665.1:g.10184617dup	GRCh37
NC_000003.10:g.10159617dup	NCBI36
NG_008212.3:g.6299dup , LRG_322:g.6299dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.511dup	ENSP00000512434.1:p.Trp171LeufsTer11
ENST00000696143.1:c.511dup	ENSP00000512435.1:p.Trp171LeufsTer11
ENST00000696153.1:c.340+746dup	ENSP00000512444.1:n.340+746dup
ENST00000256474.3:c.340+746dup MANE Select	ENSP00000256474.3:n.340+746dup
ENST00000256474.2:c.340+746dup	ENSP00000256474.2:n.340+746dup
ENST00000345392.2:c.340+746dup	ENSP00000344757.2:n.340+746dup
ENST00000477538.1:n.388dup
NM_000551.3:c.340+746dup , LRG_322t1:c.340+746dup	NP_000542.1:n.340+746dup
NM_198156.2:c.340+746dup	NP_937799.1:n.340+746dup
XM_011534078.1:c.511dup	XP_011532380.1:p.Trp171LeufsTer11
NM_001354723.1:c.511dup	NP_001341652.1:p.Trp171LeufsTer11
NM_000551.4:c.340+746dup MANE Select	NP_000542.1:n.340+746dup
NM_001354723.2:c.511dup	NP_001341652.1:p.Trp171LeufsTer11
NM_198156.3:c.340+746dup	NP_937799.1:n.340+746dup