Canonical Allele Identifier: CA2989078746
Community Standard Title: NC_000003.12:g.10141775dup
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141775dup , CM000665.2:g.10141775dup GRCh38
NC_000003.11:g.10183459dup , CM000665.1:g.10183459dup GRCh37
NC_000003.10:g.10158459dup NCBI36
NG_008212.3:g.5141dup , LRG_322:g.5141dup

Transcript Alleles

HGVS Amino-acid Change
NM_000551.3:c.-73dup , LRG_322t1:c.-73dup NP_000542.1:n.-73dup
NM_001354723.1:c.-73dup NP_001341652.1:n.-73dup
NM_198156.2:c.-73dup NP_937799.1:n.-73dup
ENST00000256474.2:c.-73dup ENSP00000256474.2:n.-73dup
XM_011534078.1:c.-73dup XP_011532380.1:n.-73dup