Canonical Allele Identifier: CA2695214802
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67489363_67489364del , CM000673.2:g.67489363_67489364del GRCh38
NC_000011.9:g.67256834_67256835del , CM000673.1:g.67256834_67256835del GRCh37
NC_000011.8:g.67013410_67013411del NCBI36
NG_008969.1:g.11330_11331del , LRG_460:g.11330_11331del

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.353_354del
ENST00000528641.7:c.280-675_280-674del ENSP00000434982.3:n.280-675_280-674del
ENST00000529797.2:n.306_307del
ENST00000682324.1:c.376_377del ENSP00000508017.1:p.Gln126AspfsTer3
ENST00000682659.1:c.100-675_100-674del ENSP00000507351.1:n.100-675_100-674del
ENST00000682699.1:c.376_377del ENSP00000507935.1:p.Gln126AspfsTer3
ENST00000683237.1:c.376_377del ENSP00000507343.1:p.Gln126AspfsTer3
ENST00000683856.1:c.199_200del ENSP00000507979.1:p.Gln67AspfsTer3
ENST00000684006.1:c.376_377del ENSP00000507269.1:p.Gln126AspfsTer3
ENST00000684657.1:c.196_197del ENSP00000507961.1:p.Gln66AspfsTer3
ENST00000279146.8:c.376_377del MANE Select ENSP00000279146.3:p.Gln126AspfsTer3
ENST00000279146.7:c.376_377del ENSP00000279146.3:p.Gln126AspfsTer3
ENST00000525341.1:c.28_29del ENSP00000476993.1:p.Gln10AspfsTer3
ENST00000528641.6:c.280-675_280-674del ENSP00000434982.2:n.280-675_280-674del
ENST00000529797.1:n.486_487del
NM_001302959.1:c.199_200del NP_001289888.1:p.Gln67AspfsTer3
NM_001302960.1:c.376_377del NP_001289889.1:p.Gln126AspfsTer3
NM_003977.3:c.376_377del NP_003968.3:p.Gln126AspfsTer3
XM_024448761.1:c.376_377del XP_024304529.1:p.Gln126AspfsTer3
NM_003977.4:c.376_377del MANE Select NP_003968.3:p.Gln126AspfsTer3
NM_001302960.2:c.376_377del NP_001289889.1:p.Gln126AspfsTer3
NM_001302959.2:c.199_200del NP_001289888.1:p.Gln67AspfsTer3