Canonical Allele Identifier: CA1345064236
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141639_10141643delinsGCCTC , CM000665.2:g.10141639_10141643delinsGCCTC GRCh38
NC_000003.11:g.10183323_10183327delinsGCCTC , CM000665.1:g.10183323_10183327delinsGCCTC GRCh37
NC_000003.10:g.10158323_10158327delinsGCCTC NCBI36
NG_008212.3:g.5005_5009delinsGCCTC , LRG_322:g.5005_5009delinsGCCTC

Transcript Alleles

HGVS Amino-acid change
ENST00000256474.2:c.-209_-205delinsGCCTC ENSP00000256474.2:n.-209_-205delinsGCCTC
NM_000551.3:c.-209_-205delinsGCCTC , LRG_322t1:c.-209_-205delinsGCCTC NP_000542.1:n.-209_-205delinsGCCTC
NM_198156.2:c.-209_-205delinsGCCTC NP_937799.1:n.-209_-205delinsGCCTC
NM_001354723.1:c.-209_-205delinsGCCTC NP_001341652.1:n.-209_-205delinsGCCTC