Canonical Allele Identifier: CA351756137

Gene: VHL

Linked Data

• COSMIC: COSM36342
• MyVariant Identifiers: chr3:g.10191495T>A (hg19) ; chr3:g.10149811T>A (hg38)
• CIViC: CA351756137

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149811T>A , CM000665.2:g.10149811T>A	GRCh38
NC_000003.11:g.10191495T>A , CM000665.1:g.10191495T>A	GRCh37
NC_000003.10:g.10166495T>A	NCBI36
NG_008212.3:g.13177T>A , LRG_322:g.13177T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*165T>A	ENSP00000512434.1:n.*165T>A
ENST00000696143.1:c.624T>A	ENSP00000512435.1:n.624T>A
ENST00000696153.1:c.599T>A	ENSP00000512444.1:p.Leu200His
ENST00000256474.3:c.488T>A MANE Select	ENSP00000256474.3:p.Leu163His
ENST00000256474.2:c.488T>A	ENSP00000256474.2:p.Leu163His
ENST00000345392.2:c.365T>A	ENSP00000344757.2:p.Leu122His
ENST00000477538.1:n.624T>A
NM_000551.3:c.488T>A , LRG_322t1:c.488T>A	NP_000542.1:p.Leu163His
NM_198156.2:c.365T>A	NP_937799.1:p.Leu122His
NM_001354723.1:c.*42T>A	NP_001341652.1:n.*42T>A
NM_000551.4:c.488T>A MANE Select	NP_000542.1:p.Leu163His
NM_001354723.2:c.*42T>A	NP_001341652.1:n.*42T>A
NM_198156.3:c.365T>A	NP_937799.1:p.Leu122His