Canonical Allele Identifier: CA3266346882
Community Standard Title: NC_000003.12:g.10142086_10142190del
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10142086_10142190del , CM000665.2:g.10142086_10142190del GRCh38
NC_000003.11:g.10183770_10183874del , CM000665.1:g.10183770_10183874del GRCh37
NC_000003.10:g.10158770_10158874del NCBI36
NG_008212.3:g.5452_5556del , LRG_322:g.5452_5556del

Transcript Alleles

HGVS Amino-acid Change
NM_000551.3:c.239_340+3del , LRG_322t1:c.239_340+3del
NM_000551.4:c.239_340+3del
NM_001354723.1:c.239_340+3del
NM_001354723.2:c.239_340+3del
NM_198156.2:c.239_340+3del
NM_198156.3:c.239_340+3del
ENST00000256474.2:c.239_340+3del
ENST00000256474.3:c.239_340+3del
ENST00000345392.2:c.239_340+3del
ENST00000696142.1:c.239_340+3del
ENST00000696143.1:c.239_340+3del
ENST00000696153.1:c.239_340+3del
XM_011534078.1:c.239_340+3del