Canonical Allele Identifier: CA1345067300

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142868A= , CM000665.2:g.10142868A=	GRCh38
NC_000003.11:g.10184552A= , CM000665.1:g.10184552A=	GRCh37
NC_000003.10:g.10159552A=	NCBI36
NG_008212.3:g.6234A= , LRG_322:g.6234A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.446A=	ENSP00000512434.1:p.His149=
ENST00000696143.1:c.446A=	ENSP00000512435.1:p.His149=
ENST00000696153.1:c.340+681A=	ENSP00000512444.1:n.340+681A=
ENST00000256474.3:c.340+681A= MANE Select	ENSP00000256474.3:n.340+681A=
ENST00000256474.2:c.340+681A=	ENSP00000256474.2:n.340+681A=
ENST00000345392.2:c.340+681A=	ENSP00000344757.2:n.340+681A=
ENST00000477538.1:n.323A=
NM_000551.3:c.340+681A= , LRG_322t1:c.340+681A=	NP_000542.1:n.340+681A=
NM_198156.2:c.340+681A=	NP_937799.1:n.340+681A=
XM_011534078.1:c.446A=	XP_011532380.1:p.His149=
NM_001354723.1:c.446A=	NP_001341652.1:p.His149=
NM_000551.4:c.340+681A= MANE Select	NP_000542.1:n.340+681A=
NM_001354723.2:c.446A=	NP_001341652.1:p.His149=
NM_198156.3:c.340+681A=	NP_937799.1:n.340+681A=