Canonical Allele Identifier: CA1345063449

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10150255G= , CM000665.2:g.10150255G=	GRCh38
NC_000003.11:g.10191939G= , CM000665.1:g.10191939G=	GRCh37
NC_000003.10:g.10166939G=	NCBI36
NG_008212.3:g.13621G= , LRG_322:g.13621G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*609G=	ENSP00000512434.1:n.*609G=
ENST00000696143.1:c.1068G=	ENSP00000512435.1:n.1068G=
ENST00000696153.1:c.*290G=	ENSP00000512444.1:n.*290G=
ENST00000256474.3:c.*290G= MANE Select	ENSP00000256474.3:n.*290G=
ENST00000256474.2:c.*290G=	ENSP00000256474.2:n.*290G=
ENST00000345392.2:c.*290G=	ENSP00000344757.2:n.*290G=
NM_000551.3:c.*290G= , LRG_322t1:c.*290G=	NP_000542.1:n.*290G=
NM_198156.2:c.*290G=	NP_937799.1:n.*290G=
NM_001354723.1:c.*486G=	NP_001341652.1:n.*486G=
NM_000551.4:c.*290G= MANE Select	NP_000542.1:n.*290G=
NM_001354723.2:c.*486G=	NP_001341652.1:n.*486G=
NM_198156.3:c.*290G=	NP_937799.1:n.*290G=