Canonical Allele Identifier: CA357055

Gene: VHL

Linked Data

• ClinVar Variation Id: 223178
• ClinVar RCV Id: RCV000208817
• dbSNP Id: rs869025625
• MyVariant Identifiers: chr3:g.10183827dupC (hg19) ; chr3:g.10142143dupC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142143dup , CM000665.2:g.10142143dup	GRCh38
NC_000003.11:g.10183827dup , CM000665.1:g.10183827dup	GRCh37
NC_000003.10:g.10158827dup	NCBI36
NG_008212.3:g.5509dup , LRG_322:g.5509dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.296dup	ENSP00000512434.1:p.Thr100AsnfsTer?
ENST00000696143.1:c.296dup	ENSP00000512435.1:p.Thr100AsnfsTer?
ENST00000696153.1:c.296dup	ENSP00000512444.1:p.Thr100AsnfsTer?
ENST00000256474.3:c.296dup MANE Select	ENSP00000256474.3:p.Thr100AsnfsTer?
ENST00000256474.2:c.296dup	ENSP00000256474.2:p.Thr100AsnfsTer?
ENST00000345392.2:c.296dup	ENSP00000344757.2:p.Thr100AsnfsTer?
NM_000551.3:c.296dup , LRG_322t1:c.296dup	NP_000542.1:p.Thr100AsnfsTer?
NM_198156.2:c.296dup	NP_937799.1:p.Thr100AsnfsTer?
XM_011534078.1:c.296dup	XP_011532380.1:p.Thr100AsnfsTer?
NM_001354723.1:c.296dup	NP_001341652.1:p.Thr100AsnfsTer?
NM_000551.4:c.296dup MANE Select	NP_000542.1:p.Thr100AsnfsTer?
NM_001354723.2:c.296dup	NP_001341652.1:p.Thr100AsnfsTer?
NM_198156.3:c.296dup	NP_937799.1:p.Thr100AsnfsTer?