Canonical Allele Identifier: CA432423193

Gene: VHL

Linked Data

• MyVariant Identifiers: chr3:g.10191496C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149812C>A , CM000665.2:g.10149812C>A	GRCh38
NC_000003.11:g.10191496C>A , CM000665.1:g.10191496C>A	GRCh37
NC_000003.10:g.10166496C>A	NCBI36
NG_008212.3:g.13178C>A , LRG_322:g.13178C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*166C>A	ENSP00000512434.1:n.*166C>A
ENST00000696143.1:c.625C>A	ENSP00000512435.1:n.625C>A
ENST00000696153.1:c.600C>A	ENSP00000512444.1:p.Leu200=
ENST00000256474.3:c.489C>A MANE Select	ENSP00000256474.3:p.Leu163=
ENST00000256474.2:c.489C>A	ENSP00000256474.2:p.Leu163=
ENST00000345392.2:c.366C>A	ENSP00000344757.2:p.Leu122=
ENST00000477538.1:n.625C>A
NM_000551.3:c.489C>A , LRG_322t1:c.489C>A	NP_000542.1:p.Leu163=
NM_198156.2:c.366C>A	NP_937799.1:p.Leu122=
NM_001354723.1:c.*43C>A	NP_001341652.1:n.*43C>A
NM_000551.4:c.489C>A MANE Select	NP_000542.1:p.Leu163=
NM_001354723.2:c.*43C>A	NP_001341652.1:n.*43C>A
NM_198156.3:c.366C>A	NP_937799.1:p.Leu122=