Canonical Allele Identifier: CA2701969117

Gene: VHL

Linked Data

• dbSNP Id: rs1413594093

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10148459C>A , CM000665.2:g.10148459C>A	GRCh38
NC_000003.11:g.10190143C>A , CM000665.1:g.10190143C>A	GRCh37
NC_000003.10:g.10165143C>A	NCBI36
NG_008212.3:g.11825C>A , LRG_322:g.11825C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*141-1328C>A	ENSP00000512434.1:n.*141-1328C>A
ENST00000696143.1:c.600-1328C>A	ENSP00000512435.1:n.600-1328C>A
ENST00000696153.1:c.464-245C>A	ENSP00000512444.1:n.464-245C>A
ENST00000256474.3:c.464-1328C>A MANE Select	ENSP00000256474.3:n.464-1328C>A
ENST00000256474.2:c.464-1328C>A	ENSP00000256474.2:n.464-1328C>A
ENST00000345392.2:c.341-1328C>A	ENSP00000344757.2:n.341-1328C>A
ENST00000477538.1:n.600-1328C>A
NM_000551.3:c.464-1328C>A , LRG_322t1:c.464-1328C>A	NP_000542.1:n.464-1328C>A
NM_198156.2:c.341-1328C>A	NP_937799.1:n.341-1328C>A
NM_001354723.1:c.*18-1328C>A	NP_001341652.1:n.*18-1328C>A
NM_000551.4:c.464-1328C>A MANE Select	NP_000542.1:n.464-1328C>A
NM_001354723.2:c.*18-1328C>A	NP_001341652.1:n.*18-1328C>A
NM_198156.3:c.341-1328C>A	NP_937799.1:n.341-1328C>A