Canonical Allele Identifier: CA1980172812
Gene: AIP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67491122_67491123delinsCT , CM000673.2:g.67491122_67491123delinsCT GRCh38
NC_000011.9:g.67258593_67258594delinsCT , CM000673.1:g.67258593_67258594delinsCT GRCh37
NC_000011.8:g.67015169_67015170delinsCT NCBI36
NG_008969.1:g.13089_13090delinsCT , LRG_460:g.13089_13090delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000684657.1:c.*129_*130delinsCT ENSP00000507961.1:n.*129_*130delinsCT
Search 100 bp 5'
Search 100 bp 3'