Canonical Allele Identifier: CA645524961

Gene: VHL

Linked Data

• COSMIC: COSM17903 ; COSM18153
• CIViC: CA645524961

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10146595_10146601del , CM000665.2:g.10146595_10146601del	GRCh38
NC_000003.11:g.10188279_10188285del , CM000665.1:g.10188279_10188285del	GRCh37
NC_000003.10:g.10163279_10163285del	NCBI36
NG_008212.3:g.9961_9967del , LRG_322:g.9961_9967del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*99_*105del	ENSP00000512434.1:n.*99_*105del
ENST00000696143.1:c.600-3192_600-3186del	ENSP00000512435.1:n.600-3192_600-3186del
ENST00000696153.1:c.422_428del	ENSP00000512444.1:p.Asn141ThrfsTer26
ENST00000256474.3:c.422_428del MANE Select	ENSP00000256474.3:p.Asn141ThrfsTer16
ENST00000256474.2:c.422_428del	ENSP00000256474.2:p.Asn141ThrfsTer16
ENST00000345392.2:c.341-3192_341-3186del	ENSP00000344757.2:n.341-3192_341-3186del
ENST00000477538.1:n.558_564del
NM_000551.3:c.422_428del , LRG_322t1:c.422_428del	NP_000542.1:p.Asn141ThrfsTer16
NM_198156.2:c.341-3192_341-3186del	NP_937799.1:n.341-3192_341-3186del
XM_011534078.1:c.*99_*105del	XP_011532380.1:n.*99_*105del
NM_001354723.1:c.*18-3192_*18-3186del	NP_001341652.1:n.*18-3192_*18-3186del
NM_000551.4:c.422_428del MANE Select	NP_000542.1:p.Asn141ThrfsTer16
NM_001354723.2:c.*18-3192_*18-3186del	NP_001341652.1:n.*18-3192_*18-3186del
NM_198156.3:c.341-3192_341-3186del	NP_937799.1:n.341-3192_341-3186del