Canonical Allele Identifier: CA1345063579

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10150357G= , CM000665.2:g.10150357G=	GRCh38
NC_000003.11:g.10192041G= , CM000665.1:g.10192041G=	GRCh37
NC_000003.10:g.10167041G=	NCBI36
NG_008212.3:g.13723G= , LRG_322:g.13723G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*711G=	ENSP00000512434.1:n.*711G=
ENST00000696143.1:c.1170G=	ENSP00000512435.1:n.1170G=
ENST00000696153.1:c.*392G=	ENSP00000512444.1:n.*392G=
ENST00000256474.3:c.*392G= MANE Select	ENSP00000256474.3:n.*392G=
ENST00000256474.2:c.*392G=	ENSP00000256474.2:n.*392G=
ENST00000345392.2:c.*392G=	ENSP00000344757.2:n.*392G=
NM_000551.3:c.*392G= , LRG_322t1:c.*392G=	NP_000542.1:n.*392G=
NM_198156.2:c.*392G=	NP_937799.1:n.*392G=
NM_001354723.1:c.*588G=	NP_001341652.1:n.*588G=
NM_000551.4:c.*392G= MANE Select	NP_000542.1:n.*392G=
NM_001354723.2:c.*588G=	NP_001341652.1:n.*588G=
NM_198156.3:c.*392G=	NP_937799.1:n.*392G=