Canonical Allele Identifier: CA645524714

Gene: VHL

Linked Data

• COSMIC: COSM6023880

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142065_10142067del , CM000665.2:g.10142065_10142067del	GRCh38
NC_000003.11:g.10183749_10183751del , CM000665.1:g.10183749_10183751del	GRCh37
NC_000003.10:g.10158749_10158751del	NCBI36
NG_008212.3:g.5431_5433del , LRG_322:g.5431_5433del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.218_220del	ENSP00000512434.1:p.Gln73_Val74delinsLeu
ENST00000696143.1:c.218_220del	ENSP00000512435.1:p.Gln73_Val74delinsLeu
ENST00000696153.1:c.218_220del	ENSP00000512444.1:p.Gln73_Val74delinsLeu
ENST00000256474.3:c.218_220del MANE Select	ENSP00000256474.3:p.Gln73_Val74delinsLeu
ENST00000256474.2:c.218_220del	ENSP00000256474.2:p.Gln73_Val74delinsLeu
ENST00000345392.2:c.218_220del	ENSP00000344757.2:p.Gln73_Val74delinsLeu
NM_000551.3:c.218_220del , LRG_322t1:c.218_220del	NP_000542.1:p.Gln73_Val74delinsLeu
NM_198156.2:c.218_220del	NP_937799.1:p.Gln73_Val74delinsLeu
XM_011534078.1:c.218_220del	XP_011532380.1:p.Gln73_Val74delinsLeu
NM_001354723.1:c.218_220del	NP_001341652.1:p.Gln73_Val74delinsLeu
NM_000551.4:c.218_220del MANE Select	NP_000542.1:p.Gln73_Val74delinsLeu
NM_001354723.2:c.218_220del	NP_001341652.1:p.Gln73_Val74delinsLeu
NM_198156.3:c.218_220del	NP_937799.1:p.Gln73_Val74delinsLeu