Canonical Allele Identifier: CA1345065557
Gene: VHL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10152874_10152880delinsGGCTCAT , CM000665.2:g.10152874_10152880delinsGGCTCAT GRCh38
NC_000003.11:g.10194558_10194564delinsGGCTCAT , CM000665.1:g.10194558_10194564delinsGGCTCAT GRCh37
NC_000003.10:g.10169558_10169564delinsGGCTCAT NCBI36
NG_008212.3:g.16240_16246delinsGGCTCAT , LRG_322:g.16240_16246delinsGGCTCAT

Transcript Alleles

HGVS Amino-acid change
ENST00000696153.1:c.*2909_*2915delinsGGCTCAT ENSP00000512444.1:n.*2909_*2915delinsGGCTCAT
ENST00000256474.3:c.*2909_*2915delinsGGCTCAT MANE Select ENSP00000256474.3:n.*2909_*2915delinsGGCTCAT
NM_000551.3:c.*2909_*2915delinsGGCTCAT , LRG_322t1:c.*2909_*2915delinsGGCTCAT NP_000542.1:n.*2909_*2915delinsGGCTCAT
NM_198156.2:c.*2909_*2915delinsGGCTCAT NP_937799.1:n.*2909_*2915delinsGGCTCAT
NM_001354723.1:c.*3105_*3111delinsGGCTCAT NP_001341652.1:n.*3105_*3111delinsGGCTCAT
NM_000551.4:c.*2909_*2915delinsGGCTCAT MANE Select NP_000542.1:n.*2909_*2915delinsGGCTCAT
NM_001354723.2:c.*3105_*3111delinsGGCTCAT NP_001341652.1:n.*3105_*3111delinsGGCTCAT
NM_198156.3:c.*2909_*2915delinsGGCTCAT NP_937799.1:n.*2909_*2915delinsGGCTCAT
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