Canonical Allele Identifier: CA351748127

Gene: VHL

Linked Data

• ClinVar Variation Id: 2952181
• ClinVar RCV Id: RCV003815332
• MyVariant Identifiers: chr3:g.10183669G>T (hg19) ; chr3:g.10141985G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141985G>T , CM000665.2:g.10141985G>T	GRCh38
NC_000003.11:g.10183669G>T , CM000665.1:g.10183669G>T	GRCh37
NC_000003.10:g.10158669G>T	NCBI36
NG_008212.3:g.5351G>T , LRG_322:g.5351G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.138G>T	ENSP00000512434.1:p.Glu46Asp
ENST00000696143.1:c.138G>T	ENSP00000512435.1:p.Glu46Asp
ENST00000696153.1:c.138G>T	ENSP00000512444.1:p.Glu46Asp
ENST00000256474.3:c.138G>T MANE Select	ENSP00000256474.3:p.Glu46Asp
ENST00000256474.2:c.138G>T	ENSP00000256474.2:p.Glu46Asp
ENST00000345392.2:c.138G>T	ENSP00000344757.2:p.Glu46Asp
NM_000551.3:c.138G>T , LRG_322t1:c.138G>T	NP_000542.1:p.Glu46Asp
NM_198156.2:c.138G>T	NP_937799.1:p.Glu46Asp
XM_011534078.1:c.138G>T	XP_011532380.1:p.Glu46Asp
NM_001354723.1:c.138G>T	NP_001341652.1:p.Glu46Asp
NM_000551.4:c.138G>T MANE Select	NP_000542.1:p.Glu46Asp
NM_001354723.2:c.138G>T	NP_001341652.1:p.Glu46Asp
NM_198156.3:c.138G>T	NP_937799.1:p.Glu46Asp