Canonical Allele Identifier: CA1345065558

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10152875G= , CM000665.2:g.10152875G=	GRCh38
NC_000003.11:g.10194559G= , CM000665.1:g.10194559G=	GRCh37
NC_000003.10:g.10169559G=	NCBI36
NG_008212.3:g.16241G= , LRG_322:g.16241G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696153.1:c.*2910G=	ENSP00000512444.1:n.*2910G=
ENST00000256474.3:c.*2910G= MANE Select	ENSP00000256474.3:n.*2910G=
NM_000551.3:c.*2910G= , LRG_322t1:c.*2910G=	NP_000542.1:n.*2910G=
NM_198156.2:c.*2910G=	NP_937799.1:n.*2910G=
NM_001354723.1:c.*3106G=	NP_001341652.1:n.*3106G=
NM_000551.4:c.*2910G= MANE Select	NP_000542.1:n.*2910G=
NM_001354723.2:c.*3106G=	NP_001341652.1:n.*3106G=
NM_198156.3:c.*2910G=	NP_937799.1:n.*2910G=