Canonical Allele Identifier: CA645524618
Community Standard Title: NC_000003.12:g.10141777dup
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141777dup , CM000665.2:g.10141777dup GRCh38
NC_000003.11:g.10183461dup , CM000665.1:g.10183461dup GRCh37
NC_000003.10:g.10158461dup NCBI36
NG_008212.3:g.5143dup , LRG_322:g.5143dup

Transcript Alleles

HGVS Amino-acid Change
NM_000551.3:c.-71dup , LRG_322t1:c.-71dup NP_000542.1:n.-71dup
NM_001354723.1:c.-71dup NP_001341652.1:n.-71dup
NM_198156.2:c.-71dup NP_937799.1:n.-71dup
ENST00000256474.2:c.-71dup ENSP00000256474.2:n.-71dup
XM_011534078.1:c.-71dup XP_011532380.1:n.-71dup