Canonical Allele Identifier: CA1345065773

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142067_10142068delinsGT , CM000665.2:g.10142067_10142068delinsGT	GRCh38
NC_000003.11:g.10183751_10183752delinsGT , CM000665.1:g.10183751_10183752delinsGT	GRCh37
NC_000003.10:g.10158751_10158752delinsGT	NCBI36
NG_008212.3:g.5433_5434delinsGT , LRG_322:g.5433_5434delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.220_221delinsGT	ENSP00000512434.1:p.Val74=
ENST00000696143.1:c.220_221delinsGT	ENSP00000512435.1:p.Val74=
ENST00000696153.1:c.220_221delinsGT	ENSP00000512444.1:p.Val74=
ENST00000256474.3:c.220_221delinsGT MANE Select	ENSP00000256474.3:p.Val74=
ENST00000256474.2:c.220_221delinsGT	ENSP00000256474.2:p.Val74=
ENST00000345392.2:c.220_221delinsGT	ENSP00000344757.2:p.Val74=
NM_000551.3:c.220_221delinsGT , LRG_322t1:c.220_221delinsGT	NP_000542.1:p.Val74=
NM_198156.2:c.220_221delinsGT	NP_937799.1:p.Val74=
XM_011534078.1:c.220_221delinsGT	XP_011532380.1:p.Val74=
NM_001354723.1:c.220_221delinsGT	NP_001341652.1:p.Val74=
NM_000551.4:c.220_221delinsGT MANE Select	NP_000542.1:p.Val74=
NM_001354723.2:c.220_221delinsGT	NP_001341652.1:p.Val74=
NM_198156.3:c.220_221delinsGT	NP_937799.1:p.Val74=