Canonical Allele Identifier: CA1345064250
Gene: VHL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141642_10141645delinsTCCG , CM000665.2:g.10141642_10141645delinsTCCG GRCh38
NC_000003.11:g.10183326_10183329delinsTCCG , CM000665.1:g.10183326_10183329delinsTCCG GRCh37
NC_000003.10:g.10158326_10158329delinsTCCG NCBI36
NG_008212.3:g.5008_5011delinsTCCG , LRG_322:g.5008_5011delinsTCCG

Transcript Alleles

HGVS Amino-acid change
ENST00000256474.2:c.-206_-203delinsTCCG ENSP00000256474.2:n.-206_-203delinsTCCG
NM_000551.3:c.-206_-203delinsTCCG , LRG_322t1:c.-206_-203delinsTCCG NP_000542.1:n.-206_-203delinsTCCG
NM_198156.2:c.-206_-203delinsTCCG NP_937799.1:n.-206_-203delinsTCCG
NM_001354723.1:c.-206_-203delinsTCCG NP_001341652.1:n.-206_-203delinsTCCG
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