Canonical Allele Identifier: CA1345064592

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141815C= , CM000665.2:g.10141815C=	GRCh38
NC_000003.11:g.10183499C= , CM000665.1:g.10183499C=	GRCh37
NC_000003.10:g.10158499C=	NCBI36
NG_008212.3:g.5181C= , LRG_322:g.5181C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.-33C=	ENSP00000512434.1:n.-33C=
ENST00000696153.1:c.-33C=	ENSP00000512444.1:n.-33C=
ENST00000256474.3:c.-33C= MANE Select	ENSP00000256474.3:n.-33C=
ENST00000256474.2:c.-33C=	ENSP00000256474.2:n.-33C=
ENST00000345392.2:c.-33C=	ENSP00000344757.2:n.-33C=
NM_000551.3:c.-33C= , LRG_322t1:c.-33C=	NP_000542.1:n.-33C=
NM_198156.2:c.-33C=	NP_937799.1:n.-33C=
XM_011534078.1:c.-33C=	XP_011532380.1:n.-33C=
NM_001354723.1:c.-33C=	NP_001341652.1:n.-33C=
NM_000551.4:c.-33C= MANE Select	NP_000542.1:n.-33C=
NM_001354723.2:c.-33C=	NP_001341652.1:n.-33C=
NM_198156.3:c.-33C=	NP_937799.1:n.-33C=