Canonical Allele Identifier: CA1345059195

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10146895T= , CM000665.2:g.10146895T=	GRCh38
NC_000003.11:g.10188579T= , CM000665.1:g.10188579T=	GRCh37
NC_000003.10:g.10163579T=	NCBI36
NG_008212.3:g.10261T= , LRG_322:g.10261T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*140+259T=	ENSP00000512434.1:n.*140+259T=
ENST00000696143.1:c.600-2892T=	ENSP00000512435.1:n.600-2892T=
ENST00000696153.1:c.463+259T=	ENSP00000512444.1:n.463+259T=
ENST00000256474.3:c.463+259T= MANE Select	ENSP00000256474.3:n.463+259T=
ENST00000256474.2:c.463+259T=	ENSP00000256474.2:n.463+259T=
ENST00000345392.2:c.341-2892T=	ENSP00000344757.2:n.341-2892T=
ENST00000477538.1:n.599+259T=
NM_000551.3:c.463+259T= , LRG_322t1:c.463+259T=	NP_000542.1:n.463+259T=
NM_198156.2:c.341-2892T=	NP_937799.1:n.341-2892T=
NM_001354723.1:c.*18-2892T=	NP_001341652.1:n.*18-2892T=
NM_000551.4:c.463+259T= MANE Select	NP_000542.1:n.463+259T=
NM_001354723.2:c.*18-2892T=	NP_001341652.1:n.*18-2892T=
NM_198156.3:c.341-2892T=	NP_937799.1:n.341-2892T=