Canonical Allele Identifier: CA2664399796

Gene: VHL

Linked Data

• gnomAD v4: 3-10141727-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141730_10141731del , CM000665.2:g.10141730_10141731del	GRCh38
NC_000003.11:g.10183414_10183415del , CM000665.1:g.10183414_10183415del	GRCh37
NC_000003.10:g.10158414_10158415del	NCBI36
NG_008212.3:g.5096_5097del , LRG_322:g.5096_5097del

Transcript Alleles

HGVS	Amino-acid change
ENST00000256474.2:c.-118_-117del	ENSP00000256474.2:n.-118_-117del
NM_000551.3:c.-118_-117del , LRG_322t1:c.-118_-117del	NP_000542.1:n.-118_-117del
NM_198156.2:c.-118_-117del	NP_937799.1:n.-118_-117del
NM_001354723.1:c.-118_-117del	NP_001341652.1:n.-118_-117del