Canonical Allele Identifier: CA2586965643

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10146620_10146628del , CM000665.2:g.10146620_10146628del	GRCh38
NC_000003.11:g.10188304_10188312del , CM000665.1:g.10188304_10188312del	GRCh37
NC_000003.10:g.10163304_10163312del	NCBI36
NG_008212.3:g.9986_9994del , LRG_322:g.9986_9994del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*124_*132del	ENSP00000512434.1:n.*124_*132del
ENST00000696143.1:c.600-3167_600-3159del	ENSP00000512435.1:n.600-3167_600-3159del
ENST00000696153.1:c.447_455del	ENSP00000512444.1:p.Asn150_Thr152del
ENST00000256474.3:c.447_455del MANE Select	ENSP00000256474.3:p.Asn150_Thr152del
ENST00000256474.2:c.447_455del	ENSP00000256474.2:p.Asn150_Thr152del
ENST00000345392.2:c.341-3167_341-3159del	ENSP00000344757.2:n.341-3167_341-3159del
ENST00000477538.1:n.583_591del
NM_000551.3:c.447_455del , LRG_322t1:c.447_455del	NP_000542.1:p.Asn150_Thr152del
NM_198156.2:c.341-3167_341-3159del	NP_937799.1:n.341-3167_341-3159del
NM_001354723.1:c.*18-3167_*18-3159del	NP_001341652.1:n.*18-3167_*18-3159del
NM_000551.4:c.447_455del MANE Select	NP_000542.1:p.Asn150_Thr152del
NM_001354723.2:c.*18-3167_*18-3159del	NP_001341652.1:n.*18-3167_*18-3159del
NM_198156.3:c.341-3167_341-3159del	NP_937799.1:n.341-3167_341-3159del