Canonical Allele Identifier: CA1345068665

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10144487C= , CM000665.2:g.10144487C=	GRCh38
NC_000003.11:g.10186171C= , CM000665.1:g.10186171C=	GRCh37
NC_000003.10:g.10161171C=	NCBI36
NG_008212.3:g.7853C= , LRG_322:g.7853C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*17+1466C=	ENSP00000512434.1:n.*17+1466C=
ENST00000696143.1:c.599+1466C=	ENSP00000512435.1:n.599+1466C=
ENST00000696153.1:c.341-2027C=	ENSP00000512444.1:n.341-2027C=
ENST00000256474.3:c.341-2027C= MANE Select	ENSP00000256474.3:n.341-2027C=
ENST00000256474.2:c.341-2027C=	ENSP00000256474.2:n.341-2027C=
ENST00000345392.2:c.340+2300C=	ENSP00000344757.2:n.340+2300C=
ENST00000477538.1:n.476+1466C=
NM_000551.3:c.341-2027C= , LRG_322t1:c.341-2027C=	NP_000542.1:n.341-2027C=
NM_198156.2:c.340+2300C=	NP_937799.1:n.340+2300C=
XM_011534078.1:c.*17+1466C=	XP_011532380.1:n.*17+1466C=
NM_001354723.1:c.*17+1466C=	NP_001341652.1:n.*17+1466C=
NM_000551.4:c.341-2027C= MANE Select	NP_000542.1:n.341-2027C=
NM_001354723.2:c.*17+1466C=	NP_001341652.1:n.*17+1466C=
NM_198156.3:c.340+2300C=	NP_937799.1:n.340+2300C=