Canonical Allele Identifier: CA1345059006

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10146677G= , CM000665.2:g.10146677G=	GRCh38
NC_000003.11:g.10188361G= , CM000665.1:g.10188361G=	GRCh37
NC_000003.10:g.10163361G=	NCBI36
NG_008212.3:g.10043G= , LRG_322:g.10043G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*140+41G=	ENSP00000512434.1:n.*140+41G=
ENST00000696143.1:c.600-3110G=	ENSP00000512435.1:n.600-3110G=
ENST00000696153.1:c.463+41G=	ENSP00000512444.1:n.463+41G=
ENST00000256474.3:c.463+41G= MANE Select	ENSP00000256474.3:n.463+41G=
ENST00000256474.2:c.463+41G=	ENSP00000256474.2:n.463+41G=
ENST00000345392.2:c.341-3110G=	ENSP00000344757.2:n.341-3110G=
ENST00000477538.1:n.599+41G=
NM_000551.3:c.463+41G= , LRG_322t1:c.463+41G=	NP_000542.1:n.463+41G=
NM_198156.2:c.341-3110G=	NP_937799.1:n.341-3110G=
NM_001354723.1:c.*18-3110G=	NP_001341652.1:n.*18-3110G=
NM_000551.4:c.463+41G= MANE Select	NP_000542.1:n.463+41G=
NM_001354723.2:c.*18-3110G=	NP_001341652.1:n.*18-3110G=
NM_198156.3:c.341-3110G=	NP_937799.1:n.341-3110G=