Canonical Allele Identifier: CA1980144130
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67483231_67483239delinsCTCCCGGAC , CM000673.2:g.67483231_67483239delinsCTCCCGGAC GRCh38
NC_000011.9:g.67250702_67250710delinsCTCCCGGAC , CM000673.1:g.67250702_67250710delinsCTCCCGGAC GRCh37
NC_000011.8:g.67007278_67007286delinsCTCCCGGAC NCBI36
NG_008969.1:g.5198_5206delinsCTCCCGGAC , LRG_460:g.5198_5206delinsCTCCCGGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000525341.2:c.50_58delinsCTCCCGGAC
ENST00000528641.7:c.73_81delinsCTCCCGGAC ENSP00000434982.3:p.Leu25=
ENST00000529797.2:n.3_11delinsCTCCCGGAC
ENST00000682324.1:c.73_81delinsCTCCCGGAC ENSP00000508017.1:p.Leu25=
ENST00000682659.1:c.73_81delinsCTCCCGGAC ENSP00000507351.1:p.Leu25=
ENST00000682699.1:c.73_81delinsCTCCCGGAC ENSP00000507935.1:p.Leu25=
ENST00000683237.1:c.73_81delinsCTCCCGGAC ENSP00000507343.1:p.Leu25=
ENST00000684006.1:c.73_81delinsCTCCCGGAC ENSP00000507269.1:p.Leu25=
ENST00000684657.1:c.73_81delinsCTCCCGGAC ENSP00000507961.1:p.Leu25=
ENST00000279146.8:c.73_81delinsCTCCCGGAC MANE Select ENSP00000279146.3:p.Leu25=
ENST00000279146.7:c.73_81delinsCTCCCGGAC ENSP00000279146.3:p.Leu25=
ENST00000528641.6:c.73_81delinsCTCCCGGAC ENSP00000434982.2:p.Leu25=
ENST00000529797.1:n.183_191delinsCTCCCGGAC
NM_001302960.1:c.73_81delinsCTCCCGGAC NP_001289889.1:p.Leu25=
NM_003977.3:c.73_81delinsCTCCCGGAC NP_003968.3:p.Leu25=
XM_024448761.1:c.73_81delinsCTCCCGGAC XP_024304529.1:p.Leu25=
NM_003977.4:c.73_81delinsCTCCCGGAC MANE Select NP_003968.3:p.Leu25=
NM_001302960.2:c.73_81delinsCTCCCGGAC NP_001289889.1:p.Leu25=