Canonical Allele Identifier: CA357063

Gene: VHL

Linked Data

• ClinVar Variation Id: 223169
• ClinVar RCV Id: RCV000208821 ; RCV000803184
• dbSNP Id: rs5030804
• COSMIC: COSM14320
• MyVariant Identifiers: chr3:g.10183764A>T (hg19) ; chr3:g.10142080A>T (hg38)
• CIViC: CA357063

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142080A>T , CM000665.2:g.10142080A>T	GRCh38
NC_000003.11:g.10183764A>T , CM000665.1:g.10183764A>T	GRCh37
NC_000003.10:g.10158764A>T	NCBI36
NG_008212.3:g.5446A>T , LRG_322:g.5446A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.233A>T	ENSP00000512434.1:p.Asn78Ile
ENST00000696143.1:c.233A>T	ENSP00000512435.1:p.Asn78Ile
ENST00000696153.1:c.233A>T	ENSP00000512444.1:p.Asn78Ile
ENST00000256474.3:c.233A>T MANE Select	ENSP00000256474.3:p.Asn78Ile
ENST00000256474.2:c.233A>T	ENSP00000256474.2:p.Asn78Ile
ENST00000345392.2:c.233A>T	ENSP00000344757.2:p.Asn78Ile
NM_000551.3:c.233A>T , LRG_322t1:c.233A>T	NP_000542.1:p.Asn78Ile
NM_198156.2:c.233A>T	NP_937799.1:p.Asn78Ile
XM_011534078.1:c.233A>T	XP_011532380.1:p.Asn78Ile
NM_001354723.1:c.233A>T	NP_001341652.1:p.Asn78Ile
NM_000551.4:c.233A>T MANE Select	NP_000542.1:p.Asn78Ile
NM_001354723.2:c.233A>T	NP_001341652.1:p.Asn78Ile
NM_198156.3:c.233A>T	NP_937799.1:p.Asn78Ile