Canonical Allele Identifier: CA645525057

Gene: VHL

Linked Data

• COSMIC: COSM17910

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149804_10149805dup , CM000665.2:g.10149804_10149805dup	GRCh38
NC_000003.11:g.10191488_10191489dup , CM000665.1:g.10191488_10191489dup	GRCh37
NC_000003.10:g.10166488_10166489dup	NCBI36
NG_008212.3:g.13170_13171dup , LRG_322:g.13170_13171dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*158_*159dup	ENSP00000512434.1:n.*158_*159dup
ENST00000696143.1:c.617_618dup	ENSP00000512435.1:n.617_618dup
ENST00000696153.1:c.592_593dup	ENSP00000512444.1:p.Cys199AspfsTer9
ENST00000256474.3:c.481_482dup MANE Select	ENSP00000256474.3:p.Cys162AspfsTer9
ENST00000256474.2:c.481_482dup	ENSP00000256474.2:p.Cys162AspfsTer9
ENST00000345392.2:c.358_359dup	ENSP00000344757.2:p.Cys121AspfsTer9
ENST00000477538.1:n.617_618dup
NM_000551.3:c.481_482dup , LRG_322t1:c.481_482dup	NP_000542.1:p.Cys162AspfsTer9
NM_198156.2:c.358_359dup	NP_937799.1:p.Cys121AspfsTer9
NM_001354723.1:c.*35_*36dup	NP_001341652.1:n.*35_*36dup
NM_000551.4:c.481_482dup MANE Select	NP_000542.1:p.Cys162AspfsTer9
NM_001354723.2:c.*35_*36dup	NP_001341652.1:n.*35_*36dup
NM_198156.3:c.358_359dup	NP_937799.1:p.Cys121AspfsTer9