Canonical Allele Identifier: CA1345064490

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10151349A= , CM000665.2:g.10151349A=	GRCh38
NC_000003.11:g.10193033A= , CM000665.1:g.10193033A=	GRCh37
NC_000003.10:g.10168033A=	NCBI36
NG_008212.3:g.14715A= , LRG_322:g.14715A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*1703A=	ENSP00000512434.1:n.*1703A=
ENST00000696143.1:c.2162A=	ENSP00000512435.1:n.2162A=
ENST00000696153.1:c.*1384A=	ENSP00000512444.1:n.*1384A=
ENST00000256474.3:c.*1384A= MANE Select	ENSP00000256474.3:n.*1384A=
ENST00000256474.2:c.*1384A=	ENSP00000256474.2:n.*1384A=
ENST00000345392.2:c.*1384A=	ENSP00000344757.2:n.*1384A=
NM_000551.3:c.*1384A= , LRG_322t1:c.*1384A=	NP_000542.1:n.*1384A=
NM_198156.2:c.*1384A=	NP_937799.1:n.*1384A=
NM_001354723.1:c.*1580A=	NP_001341652.1:n.*1580A=
NM_000551.4:c.*1384A= MANE Select	NP_000542.1:n.*1384A=
NM_001354723.2:c.*1580A=	NP_001341652.1:n.*1580A=
NM_198156.3:c.*1384A=	NP_937799.1:n.*1384A=