Canonical Allele Identifier: CA351756032
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs2125130449
MyVariant Identifiers: chr3:g.10191471T>A (hg19) chr3:g.10149787T>A (hg38)
CIViC: CA351756032
PCER: P-CER:CA351756032/193300
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149787T>A , CM000665.2:g.10149787T>A GRCh38
NC_000003.11:g.10191471T>A , CM000665.1:g.10191471T>A GRCh37
NC_000003.10:g.10166471T>A NCBI36
NG_008212.3:g.13153T>A , LRG_322:g.13153T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*141T>A ENSP00000512434.1:n.*141T>A
ENST00000696143.1:c.600T>A ENSP00000512435.1:n.600T>A
ENST00000696153.1:c.575T>A ENSP00000512444.1:p.Val192Glu
ENST00000256474.3:c.464T>A MANE Select ENSP00000256474.3:p.Val155Glu
ENST00000256474.2:c.464T>A ENSP00000256474.2:p.Val155Glu
ENST00000345392.2:c.341T>A ENSP00000344757.2:p.Val114Glu
ENST00000477538.1:n.600T>A
NM_000551.3:c.464T>A , LRG_322t1:c.464T>A NP_000542.1:p.Val155Glu
NM_198156.2:c.341T>A NP_937799.1:p.Val114Glu
NM_001354723.1:c.*18T>A NP_001341652.1:n.*18T>A
NM_000551.4:c.464T>A MANE Select NP_000542.1:p.Val155Glu
NM_001354723.2:c.*18T>A NP_001341652.1:n.*18T>A
NM_198156.3:c.341T>A NP_937799.1:p.Val114Glu
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