Canonical Allele Identifier: CA1980172117
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67489688_67489690delinsTTC , CM000673.2:g.67489688_67489690delinsTTC GRCh38
NC_000011.9:g.67257159_67257161delinsTTC , CM000673.1:g.67257159_67257161delinsTTC GRCh37
NC_000011.8:g.67013735_67013737delinsTTC NCBI36
NG_008969.1:g.11655_11657delinsTTC , LRG_460:g.11655_11657delinsTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000525341.2:c.445+233_445+235delinsTTC
ENST00000528641.7:c.280-350_280-348delinsTTC ENSP00000434982.3:n.280-350_280-348delinsTTC
ENST00000529797.2:n.631_633delinsTTC
ENST00000682324.1:c.468+233_468+235delinsTTC ENSP00000508017.1:n.468+233_468+235delinsTTC
ENST00000682659.1:c.100-350_100-348delinsTTC ENSP00000507351.1:n.100-350_100-348delinsTTC
ENST00000682699.1:c.468+233_468+235delinsTTC ENSP00000507935.1:n.468+233_468+235delinsTTC
ENST00000683237.1:c.468+233_468+235delinsTTC ENSP00000507343.1:n.468+233_468+235delinsTTC
ENST00000683856.1:c.291+233_291+235delinsTTC ENSP00000507979.1:n.291+233_291+235delinsTTC
ENST00000684006.1:c.468+233_468+235delinsTTC ENSP00000507269.1:n.468+233_468+235delinsTTC
ENST00000684657.1:c.288+233_288+235delinsTTC ENSP00000507961.1:n.288+233_288+235delinsTTC
ENST00000279146.8:c.468+233_468+235delinsTTC MANE Select ENSP00000279146.3:n.468+233_468+235delinsTTC
ENST00000279146.7:c.468+233_468+235delinsTTC ENSP00000279146.3:n.468+233_468+235delinsTTC
ENST00000525341.1:c.120+233_120+235delinsTTC ENSP00000476993.1:n.120+233_120+235delinsTTC
ENST00000528641.6:c.280-350_280-348delinsTTC ENSP00000434982.2:n.280-350_280-348delinsTTC
NM_001302959.1:c.291+233_291+235delinsTTC NP_001289888.1:n.291+233_291+235delinsTTC
NM_001302960.1:c.468+233_468+235delinsTTC NP_001289889.1:n.468+233_468+235delinsTTC
NM_003977.3:c.468+233_468+235delinsTTC NP_003968.3:n.468+233_468+235delinsTTC
XM_024448761.1:c.468+233_468+235delinsTTC XP_024304529.1:n.468+233_468+235delinsTTC
NM_003977.4:c.468+233_468+235delinsTTC MANE Select NP_003968.3:n.468+233_468+235delinsTTC
NM_001302960.2:c.468+233_468+235delinsTTC NP_001289889.1:n.468+233_468+235delinsTTC
NM_001302959.2:c.291+233_291+235delinsTTC NP_001289888.1:n.291+233_291+235delinsTTC