Canonical Allele Identifier: CA2664399871

Gene: VHL

Linked Data

• gnomAD v4: 3-10141798-A-ACCCGCGGATCCCGCGGCGTCCGG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141803_10141825dup , CM000665.2:g.10141803_10141825dup	GRCh38
NC_000003.11:g.10183487_10183509dup , CM000665.1:g.10183487_10183509dup	GRCh37
NC_000003.10:g.10158487_10158509dup	NCBI36
NG_008212.3:g.5169_5191dup , LRG_322:g.5169_5191dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.-45_-23dup	ENSP00000512434.1:n.-45_-23dup
ENST00000696153.1:c.-45_-23dup	ENSP00000512444.1:n.-45_-23dup
ENST00000256474.3:c.-45_-23dup MANE Select	ENSP00000256474.3:n.-45_-23dup
ENST00000256474.2:c.-45_-23dup	ENSP00000256474.2:n.-45_-23dup
ENST00000345392.2:c.-45_-23dup	ENSP00000344757.2:n.-45_-23dup
NM_000551.3:c.-45_-23dup , LRG_322t1:c.-45_-23dup	NP_000542.1:n.-45_-23dup
NM_198156.2:c.-45_-23dup	NP_937799.1:n.-45_-23dup
XM_011534078.1:c.-45_-23dup	XP_011532380.1:n.-45_-23dup
NM_001354723.1:c.-45_-23dup	NP_001341652.1:n.-45_-23dup
NM_000551.4:c.-45_-23dup MANE Select	NP_000542.1:n.-45_-23dup
NM_001354723.2:c.-45_-23dup	NP_001341652.1:n.-45_-23dup
NM_198156.3:c.-45_-23dup	NP_937799.1:n.-45_-23dup