Canonical Allele Identifier: CA432423689

Gene: VHL

Linked Data

• MyVariant Identifiers: chr3:g.10191571_10191572insT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149887_10149888insT , CM000665.2:g.10149887_10149888insT	GRCh38
NC_000003.11:g.10191571_10191572insT , CM000665.1:g.10191571_10191572insT	GRCh37
NC_000003.10:g.10166571_10166572insT	NCBI36
NG_008212.3:g.13253_13254insT , LRG_322:g.13253_13254insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*241_*242insT	ENSP00000512434.1:n.*241_*242insT
ENST00000696143.1:c.700_701insT	ENSP00000512435.1:n.700_701insT
ENST00000696153.1:c.675_676insT	ENSP00000512444.1:p.Glu226Ter
ENST00000256474.3:c.564_565insT MANE Select	ENSP00000256474.3:p.Glu189Ter
ENST00000256474.2:c.564_565insT	ENSP00000256474.2:p.Glu189Ter
ENST00000345392.2:c.441_442insT	ENSP00000344757.2:p.Glu148Ter
ENST00000477538.1:n.700_701insT
NM_000551.3:c.564_565insT , LRG_322t1:c.564_565insT	NP_000542.1:p.Glu189Ter
NM_198156.2:c.441_442insT	NP_937799.1:p.Glu148Ter
NM_001354723.1:c.*118_*119insT	NP_001341652.1:n.*118_*119insT
NM_000551.4:c.564_565insT MANE Select	NP_000542.1:p.Glu189Ter
NM_001354723.2:c.*118_*119insT	NP_001341652.1:n.*118_*119insT
NM_198156.3:c.441_442insT	NP_937799.1:p.Glu148Ter