Canonical Allele Identifier: CA1345062620

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149874T= , CM000665.2:g.10149874T=	GRCh38
NC_000003.11:g.10191558T= , CM000665.1:g.10191558T=	GRCh37
NC_000003.10:g.10166558T=	NCBI36
NG_008212.3:g.13240T= , LRG_322:g.13240T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*228T=	ENSP00000512434.1:n.*228T=
ENST00000696143.1:c.687T=	ENSP00000512435.1:n.687T=
ENST00000696153.1:c.662T=	ENSP00000512444.1:p.Leu221=
ENST00000256474.3:c.551T= MANE Select	ENSP00000256474.3:p.Leu184=
ENST00000256474.2:c.551T=	ENSP00000256474.2:p.Leu184=
ENST00000345392.2:c.428T=	ENSP00000344757.2:p.Leu143=
ENST00000477538.1:n.687T=
NM_000551.3:c.551T= , LRG_322t1:c.551T=	NP_000542.1:p.Leu184=
NM_198156.2:c.428T=	NP_937799.1:p.Leu143=
NM_001354723.1:c.*105T=	NP_001341652.1:n.*105T=
NM_000551.4:c.551T= MANE Select	NP_000542.1:p.Leu184=
NM_001354723.2:c.*105T=	NP_001341652.1:n.*105T=
NM_198156.3:c.428T=	NP_937799.1:p.Leu143=