Canonical Allele Identifier: CA645524649

Gene: VHL

Linked Data

• COSMIC: COSM423171

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142014_10142052del , CM000665.2:g.10142014_10142052del	GRCh38
NC_000003.11:g.10183698_10183736del , CM000665.1:g.10183698_10183736del	GRCh37
NC_000003.10:g.10158698_10158736del	NCBI36
NG_008212.3:g.5380_5418del , LRG_322:g.5380_5418del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.167_205del	ENSP00000512434.1:p.Ala56_Arg69delinsGly
ENST00000696143.1:c.167_205del	ENSP00000512435.1:p.Ala56_Arg69delinsGly
ENST00000696153.1:c.167_205del	ENSP00000512444.1:p.Ala56_Arg69delinsGly
ENST00000256474.3:c.167_205del MANE Select	ENSP00000256474.3:p.Ala56_Arg69delinsGly
ENST00000256474.2:c.167_205del	ENSP00000256474.2:p.Ala56_Arg69delinsGly
ENST00000345392.2:c.167_205del	ENSP00000344757.2:p.Ala56_Arg69delinsGly
NM_000551.3:c.167_205del , LRG_322t1:c.167_205del	NP_000542.1:p.Ala56_Arg69delinsGly
NM_198156.2:c.167_205del	NP_937799.1:p.Ala56_Arg69delinsGly
XM_011534078.1:c.167_205del	XP_011532380.1:p.Ala56_Arg69delinsGly
NM_001354723.1:c.167_205del	NP_001341652.1:p.Ala56_Arg69delinsGly
NM_000551.4:c.167_205del MANE Select	NP_000542.1:p.Ala56_Arg69delinsGly
NM_001354723.2:c.167_205del	NP_001341652.1:p.Ala56_Arg69delinsGly
NM_198156.3:c.167_205del	NP_937799.1:p.Ala56_Arg69delinsGly