Canonical Allele Identifier: CA3266346852
Community Standard Title: NC_000003.12:g.10141971_10142190dup
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141971_10142190dup , CM000665.2:g.10141971_10142190dup GRCh38
NC_000003.11:g.10183655_10183874dup , CM000665.1:g.10183655_10183874dup GRCh37
NC_000003.10:g.10158655_10158874dup NCBI36
NG_008212.3:g.5337_5556dup , LRG_322:g.5337_5556dup

Transcript Alleles

HGVS Amino-acid Change
NM_000551.3:c.124_340+3dup , LRG_322t1:c.124_340+3dup
NM_000551.4:c.124_340+3dup
NM_001354723.1:c.124_340+3dup
NM_001354723.2:c.124_340+3dup
NM_198156.2:c.124_340+3dup
NM_198156.3:c.124_340+3dup
ENST00000256474.2:c.124_340+3dup
ENST00000256474.3:c.124_340+3dup
ENST00000345392.2:c.124_340+3dup
ENST00000696142.1:c.124_340+3dup
ENST00000696143.1:c.124_340+3dup
ENST00000696153.1:c.124_340+3dup
XM_011534078.1:c.124_340+3dup