Canonical Allele Identifier: CA351756328

Gene: VHL

Linked Data

• dbSNP Id: rs2125130664
• MyVariant Identifiers: chr3:g.10191554T>A (hg19) ; chr3:g.10149870T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149870T>A , CM000665.2:g.10149870T>A	GRCh38
NC_000003.11:g.10191554T>A , CM000665.1:g.10191554T>A	GRCh37
NC_000003.10:g.10166554T>A	NCBI36
NG_008212.3:g.13236T>A , LRG_322:g.13236T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*224T>A	ENSP00000512434.1:n.*224T>A
ENST00000696143.1:c.683T>A	ENSP00000512435.1:n.683T>A
ENST00000696153.1:c.658T>A	ENSP00000512444.1:p.Ser220Thr
ENST00000256474.3:c.547T>A MANE Select	ENSP00000256474.3:p.Ser183Thr
ENST00000256474.2:c.547T>A	ENSP00000256474.2:p.Ser183Thr
ENST00000345392.2:c.424T>A	ENSP00000344757.2:p.Ser142Thr
ENST00000477538.1:n.683T>A
NM_000551.3:c.547T>A , LRG_322t1:c.547T>A	NP_000542.1:p.Ser183Thr
NM_198156.2:c.424T>A	NP_937799.1:p.Ser142Thr
NM_001354723.1:c.*101T>A	NP_001341652.1:n.*101T>A
NM_000551.4:c.547T>A MANE Select	NP_000542.1:p.Ser183Thr
NM_001354723.2:c.*101T>A	NP_001341652.1:n.*101T>A
NM_198156.3:c.424T>A	NP_937799.1:p.Ser142Thr