Canonical Allele Identifier: CA540877687
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs1239804051

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10152458_10152460del , CM000665.2:g.10152458_10152460del GRCh38
NC_000003.11:g.10194142_10194144del , CM000665.1:g.10194142_10194144del GRCh37
NC_000003.10:g.10169142_10169144del NCBI36
NG_008212.3:g.15824_15826del , LRG_322:g.15824_15826del

Transcript Alleles

HGVS Amino-acid change
ENST00000696153.1:c.*2493_*2495del ENSP00000512444.1:n.*2493_*2495del
ENST00000256474.3:c.*2493_*2495del MANE Select ENSP00000256474.3:n.*2493_*2495del
NM_000551.3:c.*2493_*2495del , LRG_322t1:c.*2493_*2495del NP_000542.1:n.*2493_*2495del
NM_198156.2:c.*2493_*2495del NP_937799.1:n.*2493_*2495del
NM_001354723.1:c.*2689_*2691del NP_001341652.1:n.*2689_*2691del
NM_000551.4:c.*2493_*2495del MANE Select NP_000542.1:n.*2493_*2495del
NM_001354723.2:c.*2689_*2691del NP_001341652.1:n.*2689_*2691del
NM_198156.3:c.*2493_*2495del NP_937799.1:n.*2493_*2495del