Canonical Allele Identifier: CA351747014

Gene: VHL

Linked Data

• ClinVar Variation Id: 2941194
• ClinVar RCV Id: RCV003792456
• gnomAD v4: 3-10141851-C-A
• MyVariant Identifiers: chr3:g.10183535C>A (hg19) ; chr3:g.10141851C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141851C>A , CM000665.2:g.10141851C>A	GRCh38
NC_000003.11:g.10183535C>A , CM000665.1:g.10183535C>A	GRCh37
NC_000003.10:g.10158535C>A	NCBI36
NG_008212.3:g.5217C>A , LRG_322:g.5217C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.4C>A	ENSP00000512434.1:p.Pro2Thr
ENST00000696143.1:c.4C>A	ENSP00000512435.1:p.Pro2Thr
ENST00000696153.1:c.4C>A	ENSP00000512444.1:p.Pro2Thr
ENST00000256474.3:c.4C>A MANE Select	ENSP00000256474.3:p.Pro2Thr
ENST00000256474.2:c.4C>A	ENSP00000256474.2:p.Pro2Thr
ENST00000345392.2:c.4C>A	ENSP00000344757.2:p.Pro2Thr
NM_000551.3:c.4C>A , LRG_322t1:c.4C>A	NP_000542.1:p.Pro2Thr
NM_198156.2:c.4C>A	NP_937799.1:p.Pro2Thr
XM_011534078.1:c.4C>A	XP_011532380.1:p.Pro2Thr
NM_001354723.1:c.4C>A	NP_001341652.1:p.Pro2Thr
NM_000551.4:c.4C>A MANE Select	NP_000542.1:p.Pro2Thr
NM_001354723.2:c.4C>A	NP_001341652.1:p.Pro2Thr
NM_198156.3:c.4C>A	NP_937799.1:p.Pro2Thr