Canonical Allele Identifier: CA1345062315
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149817_10149828delinsTTGTCCGGAGCC , CM000665.2:g.10149817_10149828delinsTTGTCCGGAGCC GRCh38
NC_000003.11:g.10191501_10191512delinsTTGTCCGGAGCC , CM000665.1:g.10191501_10191512delinsTTGTCCGGAGCC GRCh37
NC_000003.10:g.10166501_10166512delinsTTGTCCGGAGCC NCBI36
NG_008212.3:g.13183_13194delinsTTGTCCGGAGCC , LRG_322:g.13183_13194delinsTTGTCCGGAGCC

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*171_*182delinsTTGTCCGGAGCC ENSP00000512434.1:n.*171_*182delinsTTGTCC...
ENST00000696143.1:c.630_641delinsTTGTCCGGAGCC ENSP00000512435.1:n.630_641delinsTTGTCCGG...
ENST00000696153.1:c.605_616delinsTTGTCCGGAGCC ENSP00000512444.1:p.Val202=
ENST00000256474.3:c.494_505delinsTTGTCCGGAGCC MANE Select ENSP00000256474.3:p.Val165=
ENST00000256474.2:c.494_505delinsTTGTCCGGAGCC ENSP00000256474.2:p.Val165=
ENST00000345392.2:c.371_382delinsTTGTCCGGAGCC ENSP00000344757.2:p.Val124=
ENST00000477538.1:n.630_641delinsTTGTCCGGAGCC
NM_000551.3:c.494_505delinsTTGTCCGGAGCC , LRG_322t1:c.494_505delinsTTGTCCGGAGCC NP_000542.1:p.Val165=
NM_198156.2:c.371_382delinsTTGTCCGGAGCC NP_937799.1:p.Val124=
NM_001354723.1:c.*48_*59delinsTTGTCCGGAGCC NP_001341652.1:n.*48_*59delinsTTGTCCGGAGC...
NM_000551.4:c.494_505delinsTTGTCCGGAGCC MANE Select NP_000542.1:p.Val165=
NM_001354723.2:c.*48_*59delinsTTGTCCGGAGCC NP_001341652.1:n.*48_*59delinsTTGTCCGGAGC...
NM_198156.3:c.371_382delinsTTGTCCGGAGCC NP_937799.1:p.Val124=