Canonical Allele Identifier: CA1980170026
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67482969_67482971delinsACG , CM000673.2:g.67482969_67482971delinsACG GRCh38
NC_000011.9:g.67250440_67250442delinsACG , CM000673.1:g.67250440_67250442delinsACG GRCh37
NC_000011.8:g.67007016_67007018delinsACG NCBI36
NG_008969.1:g.4936_4938delinsACG , LRG_460:g.4936_4938delinsACG

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-190_-188delinsACG ENSP00000507935.1:n.-190_-188delinsACG
XM_024448761.1:c.-190_-188delinsACG XP_024304529.1:n.-190_-188delinsACG