Canonical Allele Identifier: CA432536255
Gene: VHL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141944_10141945insG , CM000665.2:g.10141944_10141945insG GRCh38
NC_000003.11:g.10183628_10183629insG , CM000665.1:g.10183628_10183629insG GRCh37
NC_000003.10:g.10158628_10158629insG NCBI36
NG_008212.3:g.5310_5311insG , LRG_322:g.5310_5311insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.97_98insG ENSP00000512434.1:p.Ser33CysfsTer?
ENST00000696143.1:c.97_98insG ENSP00000512435.1:p.Ser33CysfsTer?
ENST00000696153.1:c.97_98insG ENSP00000512444.1:p.Ser33CysfsTer?
ENST00000256474.3:c.97_98insG MANE Select ENSP00000256474.3:p.Ser33CysfsTer?
ENST00000256474.2:c.97_98insG ENSP00000256474.2:p.Ser33CysfsTer?
ENST00000345392.2:c.97_98insG ENSP00000344757.2:p.Ser33CysfsTer?
NM_000551.3:c.97_98insG , LRG_322t1:c.97_98insG NP_000542.1:p.Ser33CysfsTer?
NM_198156.2:c.97_98insG NP_937799.1:p.Ser33CysfsTer?
XM_011534078.1:c.97_98insG XP_011532380.1:p.Ser33CysfsTer?
NM_001354723.1:c.97_98insG NP_001341652.1:p.Ser33CysfsTer?
NM_000551.4:c.97_98insG MANE Select NP_000542.1:p.Ser33CysfsTer?
NM_001354723.2:c.97_98insG NP_001341652.1:p.Ser33CysfsTer?
NM_198156.3:c.97_98insG NP_937799.1:p.Ser33CysfsTer?