Canonical Allele Identifier: CA1345068857

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10144832C= , CM000665.2:g.10144832C=	GRCh38
NC_000003.11:g.10186516C= , CM000665.1:g.10186516C=	GRCh37
NC_000003.10:g.10161516C=	NCBI36
NG_008212.3:g.8198C= , LRG_322:g.8198C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*18-1682C=	ENSP00000512434.1:n.*18-1682C=
ENST00000696143.1:c.599+1811C=	ENSP00000512435.1:n.599+1811C=
ENST00000696153.1:c.341-1682C=	ENSP00000512444.1:n.341-1682C=
ENST00000256474.3:c.341-1682C= MANE Select	ENSP00000256474.3:n.341-1682C=
ENST00000256474.2:c.341-1682C=	ENSP00000256474.2:n.341-1682C=
ENST00000345392.2:c.340+2645C=	ENSP00000344757.2:n.340+2645C=
ENST00000477538.1:n.477-1682C=
NM_000551.3:c.341-1682C= , LRG_322t1:c.341-1682C=	NP_000542.1:n.341-1682C=
NM_198156.2:c.340+2645C=	NP_937799.1:n.340+2645C=
XM_011534078.1:c.*18-1682C=	XP_011532380.1:n.*18-1682C=
NM_001354723.1:c.*17+1811C=	NP_001341652.1:n.*17+1811C=
NM_000551.4:c.341-1682C= MANE Select	NP_000542.1:n.341-1682C=
NM_001354723.2:c.*17+1811C=	NP_001341652.1:n.*17+1811C=
NM_198156.3:c.340+2645C=	NP_937799.1:n.340+2645C=