Canonical Allele Identifier: CA896164870

Gene: VHL

Linked Data

• dbSNP Id: rs1317648175
• MyVariant Identifiers: chr3:g.10190201del (hg19) ; chr3:g.10148517del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10148520del , CM000665.2:g.10148520del	GRCh38
NC_000003.11:g.10190204del , CM000665.1:g.10190204del	GRCh37
NC_000003.10:g.10165204del	NCBI36
NG_008212.3:g.11886del , LRG_322:g.11886del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*141-1267del	ENSP00000512434.1:n.*141-1267del
ENST00000696143.1:c.600-1267del	ENSP00000512435.1:n.600-1267del
ENST00000696153.1:c.464-184del	ENSP00000512444.1:n.464-184del
ENST00000256474.3:c.464-1267del MANE Select	ENSP00000256474.3:n.464-1267del
ENST00000256474.2:c.464-1267del	ENSP00000256474.2:n.464-1267del
ENST00000345392.2:c.341-1267del	ENSP00000344757.2:n.341-1267del
ENST00000477538.1:n.600-1267del
NM_000551.3:c.464-1267del , LRG_322t1:c.464-1267del	NP_000542.1:n.464-1267del
NM_198156.2:c.341-1267del	NP_937799.1:n.341-1267del
NM_001354723.1:c.*18-1267del	NP_001341652.1:n.*18-1267del
NM_000551.4:c.464-1267del MANE Select	NP_000542.1:n.464-1267del
NM_001354723.2:c.*18-1267del	NP_001341652.1:n.*18-1267del
NM_198156.3:c.341-1267del	NP_937799.1:n.341-1267del