Canonical Allele Identifier: CA1345062224

Gene: VHL

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*158C=	ENSP00000512434.1:n.*158C=
ENST00000696143.1:c.617C=	ENSP00000512435.1:n.617C=
ENST00000696153.1:c.592C=	ENSP00000512444.1:p.Arg198=
ENST00000256474.3:c.481C= MANE Select	ENSP00000256474.3:p.Arg161=
ENST00000256474.2:c.481C=	ENSP00000256474.2:p.Arg161=
ENST00000345392.2:c.358C=	ENSP00000344757.2:p.Arg120=
ENST00000477538.1:n.617C=
NM_000551.3:c.481C= , LRG_322t1:c.481C=	NP_000542.1:p.Arg161=
NM_198156.2:c.358C=	NP_937799.1:p.Arg120=
NM_001354723.1:c.*35C=	NP_001341652.1:n.*35C=
NM_000551.4:c.481C= MANE Select	NP_000542.1:p.Arg161=
NM_001354723.2:c.*35C=	NP_001341652.1:n.*35C=
NM_198156.3:c.358C=	NP_937799.1:p.Arg120=