Canonical Allele Identifier: CA1345065819
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10153259_10153263delinsCAGAG , CM000665.2:g.10153259_10153263delinsCAGAG GRCh38
NC_000003.11:g.10194943_10194947delinsCAGAG , CM000665.1:g.10194943_10194947delinsCAGAG GRCh37
NC_000003.10:g.10169943_10169947delinsCAGAG NCBI36
NG_008212.3:g.16625_16629delinsCAGAG , LRG_322:g.16625_16629delinsCAGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000696153.1:c.*3294_*3298delinsCAGAG ENSP00000512444.1:n.*3294_*3298delinsCAGAG
ENST00000256474.3:c.*3294_*3298delinsCAGAG MANE Select ENSP00000256474.3:n.*3294_*3298delinsCAGAG
NM_000551.3:c.*3294_*3298delinsCAGAG , LRG_322t1:c.*3294_*3298delinsCAGAG NP_000542.1:n.*3294_*3298delinsCAGAG
NM_198156.2:c.*3294_*3298delinsCAGAG NP_937799.1:n.*3294_*3298delinsCAGAG
NM_001354723.1:c.*3490_*3494delinsCAGAG NP_001341652.1:n.*3490_*3494delinsCAGAG
NM_000551.4:c.*3294_*3298delinsCAGAG MANE Select NP_000542.1:n.*3294_*3298delinsCAGAG
NM_001354723.2:c.*3490_*3494delinsCAGAG NP_001341652.1:n.*3490_*3494delinsCAGAG
NM_198156.3:c.*3294_*3298delinsCAGAG NP_937799.1:n.*3294_*3298delinsCAGAG