Canonical Allele Identifier: CA1345064551

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141802G= , CM000665.2:g.10141802G=	GRCh38
NC_000003.11:g.10183486G= , CM000665.1:g.10183486G=	GRCh37
NC_000003.10:g.10158486G=	NCBI36
NG_008212.3:g.5168G= , LRG_322:g.5168G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.-46G=	ENSP00000512434.1:n.-46G=
ENST00000696153.1:c.-46G=	ENSP00000512444.1:n.-46G=
ENST00000256474.3:c.-46G= MANE Select	ENSP00000256474.3:n.-46G=
ENST00000256474.2:c.-46G=	ENSP00000256474.2:n.-46G=
ENST00000345392.2:c.-46G=	ENSP00000344757.2:n.-46G=
NM_000551.3:c.-46G= , LRG_322t1:c.-46G=	NP_000542.1:n.-46G=
NM_198156.2:c.-46G=	NP_937799.1:n.-46G=
XM_011534078.1:c.-46G=	XP_011532380.1:n.-46G=
NM_001354723.1:c.-46G=	NP_001341652.1:n.-46G=
NM_000551.4:c.-46G= MANE Select	NP_000542.1:n.-46G=
NM_001354723.2:c.-46G=	NP_001341652.1:n.-46G=
NM_198156.3:c.-46G=	NP_937799.1:n.-46G=