Canonical Allele Identifier: CA2664401392

Gene: VHL

Linked Data

• gnomAD v4: 3-10151051-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10151051T>C , CM000665.2:g.10151051T>C	GRCh38
NC_000003.11:g.10192735T>C , CM000665.1:g.10192735T>C	GRCh37
NC_000003.10:g.10167735T>C	NCBI36
NG_008212.3:g.14417T>C , LRG_322:g.14417T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*1405T>C	ENSP00000512434.1:n.*1405T>C
ENST00000696143.1:c.1864T>C	ENSP00000512435.1:n.1864T>C
ENST00000696153.1:c.*1086T>C	ENSP00000512444.1:n.*1086T>C
ENST00000256474.3:c.*1086T>C MANE Select	ENSP00000256474.3:n.*1086T>C
ENST00000256474.2:c.*1086T>C	ENSP00000256474.2:n.*1086T>C
ENST00000345392.2:c.*1086T>C	ENSP00000344757.2:n.*1086T>C
NM_000551.3:c.*1086T>C , LRG_322t1:c.*1086T>C	NP_000542.1:n.*1086T>C
NM_198156.2:c.*1086T>C	NP_937799.1:n.*1086T>C
NM_001354723.1:c.*1282T>C	NP_001341652.1:n.*1282T>C
NM_000551.4:c.*1086T>C MANE Select	NP_000542.1:n.*1086T>C
NM_001354723.2:c.*1282T>C	NP_001341652.1:n.*1282T>C
NM_198156.3:c.*1086T>C	NP_937799.1:n.*1086T>C