Canonical Allele Identifier: CA351756066

Gene: VHL

Linked Data

• MyVariant Identifiers: chr3:g.10191479C>A (hg19) ; chr3:g.10149795C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149795C>A , CM000665.2:g.10149795C>A	GRCh38
NC_000003.11:g.10191479C>A , CM000665.1:g.10191479C>A	GRCh37
NC_000003.10:g.10166479C>A	NCBI36
NG_008212.3:g.13161C>A , LRG_322:g.13161C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*149C>A	ENSP00000512434.1:n.*149C>A
ENST00000696143.1:c.608C>A	ENSP00000512435.1:n.608C>A
ENST00000696153.1:c.583C>A	ENSP00000512444.1:p.Leu195Met
ENST00000256474.3:c.472C>A MANE Select	ENSP00000256474.3:p.Leu158Met
ENST00000256474.2:c.472C>A	ENSP00000256474.2:p.Leu158Met
ENST00000345392.2:c.349C>A	ENSP00000344757.2:p.Leu117Met
ENST00000477538.1:n.608C>A
NM_000551.3:c.472C>A , LRG_322t1:c.472C>A	NP_000542.1:p.Leu158Met
NM_198156.2:c.349C>A	NP_937799.1:p.Leu117Met
NM_001354723.1:c.*26C>A	NP_001341652.1:n.*26C>A
NM_000551.4:c.472C>A MANE Select	NP_000542.1:p.Leu158Met
NM_001354723.2:c.*26C>A	NP_001341652.1:n.*26C>A
NM_198156.3:c.349C>A	NP_937799.1:p.Leu117Met