Canonical Allele Identifier: CA1345069113

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10145398G= , CM000665.2:g.10145398G=	GRCh38
NC_000003.11:g.10187082G= , CM000665.1:g.10187082G=	GRCh37
NC_000003.10:g.10162082G=	NCBI36
NG_008212.3:g.8764G= , LRG_322:g.8764G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*18-1116G=	ENSP00000512434.1:n.*18-1116G=
ENST00000696143.1:c.599+2377G=	ENSP00000512435.1:n.599+2377G=
ENST00000696153.1:c.341-1116G=	ENSP00000512444.1:n.341-1116G=
ENST00000256474.3:c.341-1116G= MANE Select	ENSP00000256474.3:n.341-1116G=
ENST00000256474.2:c.341-1116G=	ENSP00000256474.2:n.341-1116G=
ENST00000345392.2:c.340+3211G=	ENSP00000344757.2:n.340+3211G=
ENST00000477538.1:n.477-1116G=
NM_000551.3:c.341-1116G= , LRG_322t1:c.341-1116G=	NP_000542.1:n.341-1116G=
NM_198156.2:c.340+3211G=	NP_937799.1:n.340+3211G=
XM_011534078.1:c.*18-1116G=	XP_011532380.1:n.*18-1116G=
NM_001354723.1:c.*17+2377G=	NP_001341652.1:n.*17+2377G=
NM_000551.4:c.341-1116G= MANE Select	NP_000542.1:n.341-1116G=
NM_001354723.2:c.*17+2377G=	NP_001341652.1:n.*17+2377G=
NM_198156.3:c.340+3211G=	NP_937799.1:n.340+3211G=