Canonical Allele Identifier: CA1345063202

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149996C= , CM000665.2:g.10149996C=	GRCh38
NC_000003.11:g.10191680C= , CM000665.1:g.10191680C=	GRCh37
NC_000003.10:g.10166680C=	NCBI36
NG_008212.3:g.13362C= , LRG_322:g.13362C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*350C=	ENSP00000512434.1:n.*350C=
ENST00000696143.1:c.809C=	ENSP00000512435.1:n.809C=
ENST00000696153.1:c.*31C=	ENSP00000512444.1:n.*31C=
ENST00000256474.3:c.*31C= MANE Select	ENSP00000256474.3:n.*31C=
ENST00000256474.2:c.*31C=	ENSP00000256474.2:n.*31C=
ENST00000345392.2:c.*31C=	ENSP00000344757.2:n.*31C=
ENST00000477538.1:n.809C=
NM_000551.3:c.*31C= , LRG_322t1:c.*31C=	NP_000542.1:n.*31C=
NM_198156.2:c.*31C=	NP_937799.1:n.*31C=
NM_001354723.1:c.*227C=	NP_001341652.1:n.*227C=
NM_000551.4:c.*31C= MANE Select	NP_000542.1:n.*31C=
NM_001354723.2:c.*227C=	NP_001341652.1:n.*227C=
NM_198156.3:c.*31C=	NP_937799.1:n.*31C=