Canonical Allele Identifier: CA2755195540
Gene: VHL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10152725_10152732del , CM000665.2:g.10152725_10152732del GRCh38
NC_000003.11:g.10194409_10194416del , CM000665.1:g.10194409_10194416del GRCh37
NC_000003.10:g.10169409_10169416del NCBI36
NG_008212.3:g.16091_16098del , LRG_322:g.16091_16098del

Transcript Alleles

HGVS Amino-acid change
ENST00000696153.1:c.*2760_*2767del ENSP00000512444.1:n.*2760_*2767del
ENST00000256474.3:c.*2760_*2767del MANE Select ENSP00000256474.3:n.*2760_*2767del
NM_000551.3:c.*2760_*2767del , LRG_322t1:c.*2760_*2767del NP_000542.1:n.*2760_*2767del
NM_198156.2:c.*2760_*2767del NP_937799.1:n.*2760_*2767del
NM_001354723.1:c.*2956_*2963del NP_001341652.1:n.*2956_*2963del
NM_000551.4:c.*2760_*2767del MANE Select NP_000542.1:n.*2760_*2767del
NM_001354723.2:c.*2956_*2963del NP_001341652.1:n.*2956_*2963del
NM_198156.3:c.*2760_*2767del NP_937799.1:n.*2760_*2767del
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