Canonical Allele Identifier: CA1345064302

Gene: VHL

Linked Data

• dbSNP Id: rs1559430689
• gnomAD v4: 3-10151125-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10151125C>T , CM000665.2:g.10151125C>T	GRCh38
NC_000003.11:g.10192809C>T , CM000665.1:g.10192809C>T	GRCh37
NC_000003.10:g.10167809C>T	NCBI36
NG_008212.3:g.14491C>T , LRG_322:g.14491C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*1479C>T	ENSP00000512434.1:n.*1479C>T
ENST00000696143.1:c.1938C>T	ENSP00000512435.1:n.1938C>T
ENST00000696153.1:c.*1160C>T	ENSP00000512444.1:n.*1160C>T
ENST00000256474.3:c.*1160C>T MANE Select	ENSP00000256474.3:n.*1160C>T
ENST00000256474.2:c.*1160C>T	ENSP00000256474.2:n.*1160C>T
ENST00000345392.2:c.*1160C>T	ENSP00000344757.2:n.*1160C>T
NM_000551.3:c.*1160C>T , LRG_322t1:c.*1160C>T	NP_000542.1:n.*1160C>T
NM_198156.2:c.*1160C>T	NP_937799.1:n.*1160C>T
NM_001354723.1:c.*1356C>T	NP_001341652.1:n.*1356C>T
NM_000551.4:c.*1160C>T MANE Select	NP_000542.1:n.*1160C>T
NM_001354723.2:c.*1356C>T	NP_001341652.1:n.*1356C>T
NM_198156.3:c.*1160C>T	NP_937799.1:n.*1160C>T