Canonical Allele Identifier: CA020355

Gene: VHL

Linked Data

• ClinVar Variation Id: 127829
• ClinVar RCV Id: RCV001854559
• dbSNP Id: rs587780077
• MyVariant Identifiers: chr3:g.10188302G>T (hg19) ; chr3:g.10146618G>T (hg38)
• PCER: P-CER:CA020355/193300
• CIViC: CA020355
• PubMed: PMID:9435426 ; PMID:23318261

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10146618G>T , CM000665.2:g.10146618G>T	GRCh38
NC_000003.11:g.10188302G>T , CM000665.1:g.10188302G>T	GRCh37
NC_000003.10:g.10163302G>T	NCBI36
NG_008212.3:g.9984G>T , LRG_322:g.9984G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*122G>T	ENSP00000512434.1:n.*122G>T
ENST00000696143.1:c.600-3169G>T	ENSP00000512435.1:n.600-3169G>T
ENST00000696153.1:c.445G>T	ENSP00000512444.1:p.Ala149Ser
ENST00000256474.3:c.445G>T MANE Select	ENSP00000256474.3:p.Ala149Ser
ENST00000256474.2:c.445G>T	ENSP00000256474.2:p.Ala149Ser
ENST00000345392.2:c.341-3169G>T	ENSP00000344757.2:n.341-3169G>T
ENST00000477538.1:n.581G>T
NM_000551.3:c.445G>T , LRG_322t1:c.445G>T	NP_000542.1:p.Ala149Ser
NM_198156.2:c.341-3169G>T	NP_937799.1:n.341-3169G>T
NM_001354723.1:c.*18-3169G>T	NP_001341652.1:n.*18-3169G>T
NM_000551.4:c.445G>T MANE Select	NP_000542.1:p.Ala149Ser
NM_001354723.2:c.*18-3169G>T	NP_001341652.1:n.*18-3169G>T
NM_198156.3:c.341-3169G>T	NP_937799.1:n.341-3169G>T