Canonical Allele Identifier: CA2664399881
Gene: VHL HGNC NCBI

Linked Data

gnomAD v4: 3-10141811-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141812del , CM000665.2:g.10141812del GRCh38
NC_000003.11:g.10183496del , CM000665.1:g.10183496del GRCh37
NC_000003.10:g.10158496del NCBI36
NG_008212.3:g.5178del , LRG_322:g.5178del

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.-36del ENSP00000512434.1:n.-36del
ENST00000696153.1:c.-36del ENSP00000512444.1:n.-36del
ENST00000256474.3:c.-36del MANE Select ENSP00000256474.3:n.-36del
ENST00000256474.2:c.-36del ENSP00000256474.2:n.-36del
ENST00000345392.2:c.-36del ENSP00000344757.2:n.-36del
NM_000551.3:c.-36del , LRG_322t1:c.-36del NP_000542.1:n.-36del
NM_198156.2:c.-36del NP_937799.1:n.-36del
XM_011534078.1:c.-36del XP_011532380.1:n.-36del
NM_001354723.1:c.-36del NP_001341652.1:n.-36del
NM_000551.4:c.-36del MANE Select NP_000542.1:n.-36del
NM_001354723.2:c.-36del NP_001341652.1:n.-36del
NM_198156.3:c.-36del NP_937799.1:n.-36del
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