Canonical Allele Identifier: CA916081412

Gene: VHL

Linked Data

• ClinVar Variation Id: 842699
• ClinVar RCV Id: RCV001045159
• dbSNP Id: rs1696160044

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142839A>C , CM000665.2:g.10142839A>C	GRCh38
NC_000003.11:g.10184523A>C , CM000665.1:g.10184523A>C	GRCh37
NC_000003.10:g.10159523A>C	NCBI36
NG_008212.3:g.6205A>C , LRG_322:g.6205A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.417A>C	ENSP00000512434.1:p.Thr139=
ENST00000696143.1:c.417A>C	ENSP00000512435.1:p.Thr139=
ENST00000696153.1:c.340+652A>C	ENSP00000512444.1:n.340+652A>C
ENST00000256474.3:c.340+652A>C MANE Select	ENSP00000256474.3:n.340+652A>C
ENST00000256474.2:c.340+652A>C	ENSP00000256474.2:n.340+652A>C
ENST00000345392.2:c.340+652A>C	ENSP00000344757.2:n.340+652A>C
ENST00000477538.1:n.294A>C
NM_000551.3:c.340+652A>C , LRG_322t1:c.340+652A>C	NP_000542.1:n.340+652A>C
NM_198156.2:c.340+652A>C	NP_937799.1:n.340+652A>C
XM_011534078.1:c.417A>C	XP_011532380.1:p.Thr139=
NM_001354723.1:c.417A>C	NP_001341652.1:p.Thr139=
NM_000551.4:c.340+652A>C MANE Select	NP_000542.1:n.340+652A>C
NM_001354723.2:c.417A>C	NP_001341652.1:p.Thr139=
NM_198156.3:c.340+652A>C	NP_937799.1:n.340+652A>C