Canonical Allele Identifier: CA1345063333

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10150126G= , CM000665.2:g.10150126G=	GRCh38
NC_000003.11:g.10191810G= , CM000665.1:g.10191810G=	GRCh37
NC_000003.10:g.10166810G=	NCBI36
NG_008212.3:g.13492G= , LRG_322:g.13492G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*480G=	ENSP00000512434.1:n.*480G=
ENST00000696143.1:c.939G=	ENSP00000512435.1:n.939G=
ENST00000696153.1:c.*161G=	ENSP00000512444.1:n.*161G=
ENST00000256474.3:c.*161G= MANE Select	ENSP00000256474.3:n.*161G=
ENST00000256474.2:c.*161G=	ENSP00000256474.2:n.*161G=
ENST00000345392.2:c.*161G=	ENSP00000344757.2:n.*161G=
ENST00000477538.1:n.939G=
NM_000551.3:c.*161G= , LRG_322t1:c.*161G=	NP_000542.1:n.*161G=
NM_198156.2:c.*161G=	NP_937799.1:n.*161G=
NM_001354723.1:c.*357G=	NP_001341652.1:n.*357G=
NM_000551.4:c.*161G= MANE Select	NP_000542.1:n.*161G=
NM_001354723.2:c.*357G=	NP_001341652.1:n.*357G=
NM_198156.3:c.*161G=	NP_937799.1:n.*161G=