Canonical Allele Identifier: CA1980170034
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67482982_67482983delinsGC , CM000673.2:g.67482982_67482983delinsGC GRCh38
NC_000011.9:g.67250453_67250454delinsGC , CM000673.1:g.67250453_67250454delinsGC GRCh37
NC_000011.8:g.67007029_67007030delinsGC NCBI36
NG_008969.1:g.4949_4950delinsGC , LRG_460:g.4949_4950delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-177_-176delinsGC ENSP00000507935.1:n.-177_-176delinsGC
XM_024448761.1:c.-177_-176delinsGC XP_024304529.1:n.-177_-176delinsGC