Canonical Allele Identifier: CA351754341

Gene: VHL

Linked Data

• dbSNP Id: rs763525739
• COSMIC: COSM4152601
• MyVariant Identifiers: chr3:g.10188307T>A (hg19) ; chr3:g.10146623T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10146623T>A , CM000665.2:g.10146623T>A	GRCh38
NC_000003.11:g.10188307T>A , CM000665.1:g.10188307T>A	GRCh37
NC_000003.10:g.10163307T>A	NCBI36
NG_008212.3:g.9989T>A , LRG_322:g.9989T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*127T>A	ENSP00000512434.1:n.*127T>A
ENST00000696143.1:c.600-3164T>A	ENSP00000512435.1:n.600-3164T>A
ENST00000696153.1:c.450T>A	ENSP00000512444.1:p.Asn150Lys
ENST00000256474.3:c.450T>A MANE Select	ENSP00000256474.3:p.Asn150Lys
ENST00000256474.2:c.450T>A	ENSP00000256474.2:p.Asn150Lys
ENST00000345392.2:c.341-3164T>A	ENSP00000344757.2:n.341-3164T>A
ENST00000477538.1:n.586T>A
NM_000551.3:c.450T>A , LRG_322t1:c.450T>A	NP_000542.1:p.Asn150Lys
NM_198156.2:c.341-3164T>A	NP_937799.1:n.341-3164T>A
NM_001354723.1:c.*18-3164T>A	NP_001341652.1:n.*18-3164T>A
NM_000551.4:c.450T>A MANE Select	NP_000542.1:p.Asn150Lys
NM_001354723.2:c.*18-3164T>A	NP_001341652.1:n.*18-3164T>A
NM_198156.3:c.341-3164T>A	NP_937799.1:n.341-3164T>A