Canonical Allele Identifier: CA1345063592

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10150363G= , CM000665.2:g.10150363G=	GRCh38
NC_000003.11:g.10192047G= , CM000665.1:g.10192047G=	GRCh37
NC_000003.10:g.10167047G=	NCBI36
NG_008212.3:g.13729G= , LRG_322:g.13729G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*717G=	ENSP00000512434.1:n.*717G=
ENST00000696143.1:c.1176G=	ENSP00000512435.1:n.1176G=
ENST00000696153.1:c.*398G=	ENSP00000512444.1:n.*398G=
ENST00000256474.3:c.*398G= MANE Select	ENSP00000256474.3:n.*398G=
ENST00000256474.2:c.*398G=	ENSP00000256474.2:n.*398G=
ENST00000345392.2:c.*398G=	ENSP00000344757.2:n.*398G=
NM_000551.3:c.*398G= , LRG_322t1:c.*398G=	NP_000542.1:n.*398G=
NM_198156.2:c.*398G=	NP_937799.1:n.*398G=
NM_001354723.1:c.*594G=	NP_001341652.1:n.*594G=
NM_000551.4:c.*398G= MANE Select	NP_000542.1:n.*398G=
NM_001354723.2:c.*594G=	NP_001341652.1:n.*594G=
NM_198156.3:c.*398G=	NP_937799.1:n.*398G=