Canonical Allele Identifier: CA645525058

Gene: VHL

Linked Data

• COSMIC: COSM17780

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149804_10149806del , CM000665.2:g.10149804_10149806del	GRCh38
NC_000003.11:g.10191488_10191490del , CM000665.1:g.10191488_10191490del	GRCh37
NC_000003.10:g.10166488_10166490del	NCBI36
NG_008212.3:g.13170_13172del , LRG_322:g.13170_13172del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*158_*160del	ENSP00000512434.1:n.*158_*160del
ENST00000696143.1:c.617_619del	ENSP00000512435.1:n.617_619del
ENST00000696153.1:c.592_594del	ENSP00000512444.1:p.Arg198del
ENST00000256474.3:c.481_483del MANE Select	ENSP00000256474.3:p.Arg161del
ENST00000256474.2:c.481_483del	ENSP00000256474.2:p.Arg161del
ENST00000345392.2:c.358_360del	ENSP00000344757.2:p.Arg120del
ENST00000477538.1:n.617_619del
NM_000551.3:c.481_483del , LRG_322t1:c.481_483del	NP_000542.1:p.Arg161del
NM_198156.2:c.358_360del	NP_937799.1:p.Arg120del
NM_001354723.1:c.*35_*37del	NP_001341652.1:n.*35_*37del
NM_000551.4:c.481_483del MANE Select	NP_000542.1:p.Arg161del
NM_001354723.2:c.*35_*37del	NP_001341652.1:n.*35_*37del
NM_198156.3:c.358_360del	NP_937799.1:p.Arg120del