Canonical Allele Identifier: CA432423880

Gene: VHL

Linked Data

• MyVariant Identifiers: chr3:g.10191613A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149929A>T , CM000665.2:g.10149929A>T	GRCh38
NC_000003.11:g.10191613A>T , CM000665.1:g.10191613A>T	GRCh37
NC_000003.10:g.10166613A>T	NCBI36
NG_008212.3:g.13295A>T , LRG_322:g.13295A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*283A>T	ENSP00000512434.1:n.*283A>T
ENST00000696143.1:c.742A>T	ENSP00000512435.1:n.742A>T
ENST00000696153.1:c.717A>T	ENSP00000512444.1:p.Thr239=
ENST00000256474.3:c.606A>T MANE Select	ENSP00000256474.3:p.Thr202=
ENST00000256474.2:c.606A>T	ENSP00000256474.2:p.Thr202=
ENST00000345392.2:c.483A>T	ENSP00000344757.2:p.Thr161=
ENST00000477538.1:n.742A>T
NM_000551.3:c.606A>T , LRG_322t1:c.606A>T	NP_000542.1:p.Thr202=
NM_198156.2:c.483A>T	NP_937799.1:p.Thr161=
NM_001354723.1:c.*160A>T	NP_001341652.1:n.*160A>T
NM_000551.4:c.606A>T MANE Select	NP_000542.1:p.Thr202=
NM_001354723.2:c.*160A>T	NP_001341652.1:n.*160A>T
NM_198156.3:c.483A>T	NP_937799.1:p.Thr161=