Canonical Allele Identifier: CA1345064737

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10151742T= , CM000665.2:g.10151742T=	GRCh38
NC_000003.11:g.10193426T= , CM000665.1:g.10193426T=	GRCh37
NC_000003.10:g.10168426T=	NCBI36
NG_008212.3:g.15108T= , LRG_322:g.15108T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*2096T=	ENSP00000512434.1:n.*2096T=
ENST00000696143.1:c.2555T=	ENSP00000512435.1:n.2555T=
ENST00000696153.1:c.*1777T=	ENSP00000512444.1:n.*1777T=
ENST00000256474.3:c.*1777T= MANE Select	ENSP00000256474.3:n.*1777T=
ENST00000256474.2:c.*1777T=	ENSP00000256474.2:n.*1777T=
ENST00000345392.2:c.*1777T=	ENSP00000344757.2:n.*1777T=
NM_000551.3:c.*1777T= , LRG_322t1:c.*1777T=	NP_000542.1:n.*1777T=
NM_198156.2:c.*1777T=	NP_937799.1:n.*1777T=
NM_001354723.1:c.*1973T=	NP_001341652.1:n.*1973T=
NM_000551.4:c.*1777T= MANE Select	NP_000542.1:n.*1777T=
NM_001354723.2:c.*1973T=	NP_001341652.1:n.*1973T=
NM_198156.3:c.*1777T=	NP_937799.1:n.*1777T=