Canonical Allele Identifier: CA1345069733
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10146516_10146517delinsCA , CM000665.2:g.10146516_10146517delinsCA GRCh38
NC_000003.11:g.10188200_10188201delinsCA , CM000665.1:g.10188200_10188201delinsCA GRCh37
NC_000003.10:g.10163200_10163201delinsCA NCBI36
NG_008212.3:g.9882_9883delinsCA , LRG_322:g.9882_9883delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*20_*21delinsCA ENSP00000512434.1:n.*20_*21delinsCA
ENST00000696143.1:c.600-3271_600-3270delinsCA ENSP00000512435.1:n.600-3271_600-3270deli...
ENST00000696153.1:c.343_344delinsCA ENSP00000512444.1:p.His115=
ENST00000256474.3:c.343_344delinsCA MANE Select ENSP00000256474.3:p.His115=
ENST00000256474.2:c.343_344delinsCA ENSP00000256474.2:p.His115=
ENST00000345392.2:c.341-3271_341-3270delinsCA ENSP00000344757.2:n.341-3271_341-3270deli...
ENST00000477538.1:n.479_480delinsCA
NM_000551.3:c.343_344delinsCA , LRG_322t1:c.343_344delinsCA NP_000542.1:p.His115=
NM_198156.2:c.341-3271_341-3270delinsCA NP_937799.1:n.341-3271_341-3270delinsCA
XM_011534078.1:c.*20_*21delinsCA XP_011532380.1:n.*20_*21delinsCA
NM_001354723.1:c.*18-3271_*18-3270delinsCA NP_001341652.1:n.*18-3271_*18-3270delinsC...
NM_000551.4:c.343_344delinsCA MANE Select NP_000542.1:p.His115=
NM_001354723.2:c.*18-3271_*18-3270delinsCA NP_001341652.1:n.*18-3271_*18-3270delinsC...
NM_198156.3:c.341-3271_341-3270delinsCA NP_937799.1:n.341-3271_341-3270delinsCA