Canonical Allele Identifier: CA2664399904
Gene: VHL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141892_10141951del , CM000665.2:g.10141892_10141951del GRCh38
NC_000003.11:g.10183576_10183635del , CM000665.1:g.10183576_10183635del GRCh37
NC_000003.10:g.10158576_10158635del NCBI36
NG_008212.3:g.5258_5317del , LRG_322:g.5258_5317del

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.45_104del ENSP00000512434.1:p.Glu16_Ala35del
ENST00000696143.1:c.45_104del ENSP00000512435.1:p.Glu16_Ala35del
ENST00000696153.1:c.45_104del ENSP00000512444.1:p.Glu16_Ala35del
ENST00000256474.3:c.45_104del MANE Select ENSP00000256474.3:p.Glu16_Ala35del
ENST00000256474.2:c.45_104del ENSP00000256474.2:p.Glu16_Ala35del
ENST00000345392.2:c.45_104del ENSP00000344757.2:p.Glu16_Ala35del
NM_000551.3:c.45_104del , LRG_322t1:c.45_104del NP_000542.1:p.Glu16_Ala35del
NM_198156.2:c.45_104del NP_937799.1:p.Glu16_Ala35del
XM_011534078.1:c.45_104del XP_011532380.1:p.Glu16_Ala35del
NM_001354723.1:c.45_104del NP_001341652.1:p.Glu16_Ala35del
NM_000551.4:c.45_104del MANE Select NP_000542.1:p.Glu16_Ala35del
NM_001354723.2:c.45_104del NP_001341652.1:p.Glu16_Ala35del
NM_198156.3:c.45_104del NP_937799.1:p.Glu16_Ala35del