Canonical Allele Identifier: CA645524741

Gene: VHL

Linked Data

• COSMIC: COSM33994

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142079_10142081dup , CM000665.2:g.10142079_10142081dup	GRCh38
NC_000003.11:g.10183763_10183765dup , CM000665.1:g.10183763_10183765dup	GRCh37
NC_000003.10:g.10158763_10158765dup	NCBI36
NG_008212.3:g.5445_5447dup , LRG_322:g.5445_5447dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.232_234dup	ENSP00000512434.1:p.Asn78_Arg79insAsn
ENST00000696143.1:c.232_234dup	ENSP00000512435.1:p.Asn78_Arg79insAsn
ENST00000696153.1:c.232_234dup	ENSP00000512444.1:p.Asn78_Arg79insAsn
ENST00000256474.3:c.232_234dup MANE Select	ENSP00000256474.3:p.Asn78_Arg79insAsn
ENST00000256474.2:c.232_234dup	ENSP00000256474.2:p.Asn78_Arg79insAsn
ENST00000345392.2:c.232_234dup	ENSP00000344757.2:p.Asn78_Arg79insAsn
NM_000551.3:c.232_234dup , LRG_322t1:c.232_234dup	NP_000542.1:p.Asn78_Arg79insAsn
NM_198156.2:c.232_234dup	NP_937799.1:p.Asn78_Arg79insAsn
XM_011534078.1:c.232_234dup	XP_011532380.1:p.Asn78_Arg79insAsn
NM_001354723.1:c.232_234dup	NP_001341652.1:p.Asn78_Arg79insAsn
NM_000551.4:c.232_234dup MANE Select	NP_000542.1:p.Asn78_Arg79insAsn
NM_001354723.2:c.232_234dup	NP_001341652.1:p.Asn78_Arg79insAsn
NM_198156.3:c.232_234dup	NP_937799.1:p.Asn78_Arg79insAsn