Canonical Allele Identifier: CA16621940
Gene: VHL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149802_10149803del , CM000665.2:g.10149802_10149803del GRCh38
NC_000003.11:g.10191486_10191487del , CM000665.1:g.10191486_10191487del GRCh37
NC_000003.10:g.10166486_10166487del NCBI36
NG_008212.3:g.13168_13169del , LRG_322:g.13168_13169del

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*156_*157del ENSP00000512434.1:n.*156_*157del
ENST00000696143.1:c.615_616del ENSP00000512435.1:n.615_616del
ENST00000696153.1:c.590_591del ENSP00000512444.1:p.Glu197AlafsTer13
ENST00000256474.3:c.479_480del MANE Select ENSP00000256474.3:p.Glu160AlafsTer13
ENST00000256474.2:c.479_480del ENSP00000256474.2:p.Glu160AlafsTer13
ENST00000345392.2:c.356_357del ENSP00000344757.2:p.Glu119AlafsTer13
ENST00000477538.1:n.615_616del
NM_000551.3:c.479_480del , LRG_322t1:c.479_480del NP_000542.1:p.Glu160AlafsTer13
NM_198156.2:c.356_357del NP_937799.1:p.Glu119AlafsTer13
NM_001354723.1:c.*33_*34del NP_001341652.1:n.*33_*34del
NM_000551.4:c.479_480del MANE Select NP_000542.1:p.Glu160AlafsTer13
NM_001354723.2:c.*33_*34del NP_001341652.1:n.*33_*34del
NM_198156.3:c.356_357del NP_937799.1:p.Glu119AlafsTer13