Canonical Allele Identifier: CA2838175231

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10151025C>G , CM000665.2:g.10151025C>G	GRCh38
NC_000003.11:g.10192709C>G , CM000665.1:g.10192709C>G	GRCh37
NC_000003.10:g.10167709C>G	NCBI36
NG_008212.3:g.14391C>G , LRG_322:g.14391C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*1379C>G	ENSP00000512434.1:n.*1379C>G
ENST00000696143.1:c.1838C>G	ENSP00000512435.1:n.1838C>G
ENST00000696153.1:c.*1060C>G	ENSP00000512444.1:n.*1060C>G
ENST00000256474.3:c.*1060C>G MANE Select	ENSP00000256474.3:n.*1060C>G
ENST00000256474.2:c.*1060C>G	ENSP00000256474.2:n.*1060C>G
ENST00000345392.2:c.*1060C>G	ENSP00000344757.2:n.*1060C>G
NM_000551.3:c.*1060C>G , LRG_322t1:c.*1060C>G	NP_000542.1:n.*1060C>G
NM_198156.2:c.*1060C>G	NP_937799.1:n.*1060C>G
NM_001354723.1:c.*1256C>G	NP_001341652.1:n.*1256C>G
NM_000551.4:c.*1060C>G MANE Select	NP_000542.1:n.*1060C>G
NM_001354723.2:c.*1256C>G	NP_001341652.1:n.*1256C>G
NM_198156.3:c.*1060C>G	NP_937799.1:n.*1060C>G