Canonical Allele Identifier: CA1345062897

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149916T= , CM000665.2:g.10149916T=	GRCh38
NC_000003.11:g.10191600T= , CM000665.1:g.10191600T=	GRCh37
NC_000003.10:g.10166600T=	NCBI36
NG_008212.3:g.13282T= , LRG_322:g.13282T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*270T=	ENSP00000512434.1:n.*270T=
ENST00000696143.1:c.729T=	ENSP00000512435.1:n.729T=
ENST00000696153.1:c.704T=	ENSP00000512444.1:p.Leu235=
ENST00000256474.3:c.593T= MANE Select	ENSP00000256474.3:p.Leu198=
ENST00000256474.2:c.593T=	ENSP00000256474.2:p.Leu198=
ENST00000345392.2:c.470T=	ENSP00000344757.2:p.Leu157=
ENST00000477538.1:n.729T=
NM_000551.3:c.593T= , LRG_322t1:c.593T=	NP_000542.1:p.Leu198=
NM_198156.2:c.470T=	NP_937799.1:p.Leu157=
NM_001354723.1:c.*147T=	NP_001341652.1:n.*147T=
NM_000551.4:c.593T= MANE Select	NP_000542.1:p.Leu198=
NM_001354723.2:c.*147T=	NP_001341652.1:n.*147T=
NM_198156.3:c.470T=	NP_937799.1:p.Leu157=