Canonical Allele Identifier: CA1345059725

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10147491G= , CM000665.2:g.10147491G=	GRCh38
NC_000003.11:g.10189175G= , CM000665.1:g.10189175G=	GRCh37
NC_000003.10:g.10164175G=	NCBI36
NG_008212.3:g.10857G= , LRG_322:g.10857G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*140+855G=	ENSP00000512434.1:n.*140+855G=
ENST00000696143.1:c.600-2296G=	ENSP00000512435.1:n.600-2296G=
ENST00000696153.1:c.463+855G=	ENSP00000512444.1:n.463+855G=
ENST00000256474.3:c.463+855G= MANE Select	ENSP00000256474.3:n.463+855G=
ENST00000256474.2:c.463+855G=	ENSP00000256474.2:n.463+855G=
ENST00000345392.2:c.341-2296G=	ENSP00000344757.2:n.341-2296G=
ENST00000477538.1:n.599+855G=
NM_000551.3:c.463+855G= , LRG_322t1:c.463+855G=	NP_000542.1:n.463+855G=
NM_198156.2:c.341-2296G=	NP_937799.1:n.341-2296G=
NM_001354723.1:c.*18-2296G=	NP_001341652.1:n.*18-2296G=
NM_000551.4:c.463+855G= MANE Select	NP_000542.1:n.463+855G=
NM_001354723.2:c.*18-2296G=	NP_001341652.1:n.*18-2296G=
NM_198156.3:c.341-2296G=	NP_937799.1:n.341-2296G=