Canonical Allele Identifier: CA645524851

Gene: VHL

Linked Data

• COSMIC: COSM17893

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142175_10142178dup , CM000665.2:g.10142175_10142178dup	GRCh38
NC_000003.11:g.10183859_10183862dup , CM000665.1:g.10183859_10183862dup	GRCh37
NC_000003.10:g.10158859_10158862dup	NCBI36
NG_008212.3:g.5541_5544dup , LRG_322:g.5541_5544dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.328_331dup	ENSP00000512434.1:p.Ser111ThrfsTer?
ENST00000696143.1:c.328_331dup	ENSP00000512435.1:p.Ser111ThrfsTer?
ENST00000696153.1:c.328_331dup	ENSP00000512444.1:p.Ser111ThrfsTer22
ENST00000256474.3:c.328_331dup MANE Select	ENSP00000256474.3:p.Ser111ThrfsTer22
ENST00000256474.2:c.328_331dup	ENSP00000256474.2:p.Ser111ThrfsTer22
ENST00000345392.2:c.328_331dup	ENSP00000344757.2:p.Ser111ThrfsTer23
NM_000551.3:c.328_331dup , LRG_322t1:c.328_331dup	NP_000542.1:p.Ser111ThrfsTer22
NM_198156.2:c.328_331dup	NP_937799.1:p.Ser111ThrfsTer23
XM_011534078.1:c.328_331dup	XP_011532380.1:p.Ser111ThrfsTer?
NM_001354723.1:c.328_331dup	NP_001341652.1:p.Ser111ThrfsTer?
NM_000551.4:c.328_331dup MANE Select	NP_000542.1:p.Ser111ThrfsTer22
NM_001354723.2:c.328_331dup	NP_001341652.1:p.Ser111ThrfsTer?
NM_198156.3:c.328_331dup	NP_937799.1:p.Ser111ThrfsTer23