Canonical Allele Identifier: CA2573320481
Community Standard Title: NM_000551.4(VHL):c.174_191del (p.Pro59_Arg64del)
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10142021_10142038del , CM000665.2:g.10142021_10142038del GRCh38
NC_000003.11:g.10183705_10183722del , CM000665.1:g.10183705_10183722del GRCh37
NC_000003.10:g.10158705_10158722del NCBI36
NG_008212.3:g.5387_5404del , LRG_322:g.5387_5404del

Transcript Alleles

HGVS Amino-acid Change
NM_000551.4:c.174_191del MANE Select NP_000542.1:p.Pro59_Arg64del
ENST00000256474.3:c.174_191del MANE Select ENSP00000256474.3:p.Pro59_Arg64del
NM_000551.3:c.174_191del , LRG_322t1:c.174_191del NP_000542.1:p.Pro59_Arg64del
NM_001354723.1:c.174_191del NP_001341652.1:p.Pro59_Arg64del
NM_001354723.2:c.174_191del NP_001341652.1:p.Pro59_Arg64del
NM_198156.2:c.174_191del NP_937799.1:p.Pro59_Arg64del
NM_198156.3:c.174_191del NP_937799.1:p.Pro59_Arg64del
ENST00000256474.2:c.174_191del ENSP00000256474.2:p.Pro59_Arg64del
ENST00000345392.2:c.174_191del ENSP00000344757.2:p.Pro59_Arg64del
ENST00000696142.1:c.174_191del ENSP00000512434.1:p.Pro59_Arg64del
ENST00000696143.1:c.174_191del ENSP00000512435.1:p.Pro59_Arg64del
ENST00000696153.1:c.174_191del ENSP00000512444.1:p.Pro59_Arg64del
XM_011534078.1:c.174_191del XP_011532380.1:p.Pro59_Arg64del