Canonical Allele Identifier: CA432423080

Gene: VHL

Linked Data

• MyVariant Identifiers: chr3:g.10191478T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149794T>G , CM000665.2:g.10149794T>G	GRCh38
NC_000003.11:g.10191478T>G , CM000665.1:g.10191478T>G	GRCh37
NC_000003.10:g.10166478T>G	NCBI36
NG_008212.3:g.13160T>G , LRG_322:g.13160T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*148T>G	ENSP00000512434.1:n.*148T>G
ENST00000696143.1:c.607T>G	ENSP00000512435.1:n.607T>G
ENST00000696153.1:c.582T>G	ENSP00000512444.1:p.Thr194=
ENST00000256474.3:c.471T>G MANE Select	ENSP00000256474.3:p.Thr157=
ENST00000256474.2:c.471T>G	ENSP00000256474.2:p.Thr157=
ENST00000345392.2:c.348T>G	ENSP00000344757.2:p.Thr116=
ENST00000477538.1:n.607T>G
NM_000551.3:c.471T>G , LRG_322t1:c.471T>G	NP_000542.1:p.Thr157=
NM_198156.2:c.348T>G	NP_937799.1:p.Thr116=
NM_001354723.1:c.*25T>G	NP_001341652.1:n.*25T>G
NM_000551.4:c.471T>G MANE Select	NP_000542.1:p.Thr157=
NM_001354723.2:c.*25T>G	NP_001341652.1:n.*25T>G
NM_198156.3:c.348T>G	NP_937799.1:p.Thr116=