Canonical Allele Identifier: CA1980172298
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490110_67490111delinsCT , CM000673.2:g.67490110_67490111delinsCT GRCh38
NC_000011.9:g.67257581_67257582delinsCT , CM000673.1:g.67257581_67257582delinsCT GRCh37
NC_000011.8:g.67014157_67014158delinsCT NCBI36
NG_008969.1:g.12077_12078delinsCT , LRG_460:g.12077_12078delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000525341.2:c.518_519delinsCT
ENST00000528641.7:c.352_353delinsCT ENSP00000434982.3:p.Leu118=
ENST00000529797.2:n.1053_1054delinsCT
ENST00000682324.1:c.468+655_468+656delinsCT ENSP00000508017.1:n.468+655_468+656delinsCT
ENST00000682659.1:c.172_173delinsCT ENSP00000507351.1:p.Leu58=
ENST00000682699.1:c.541_542delinsCT ENSP00000507935.1:p.Leu181=
ENST00000683237.1:c.541_542delinsCT ENSP00000507343.1:p.Leu181=
ENST00000683856.1:c.364_365delinsCT ENSP00000507979.1:p.Leu122=
ENST00000684006.1:c.541_542delinsCT ENSP00000507269.1:p.Leu181=
ENST00000684657.1:c.361_362delinsCT ENSP00000507961.1:p.Leu121=
ENST00000279146.8:c.541_542delinsCT MANE Select ENSP00000279146.3:p.Leu181=
ENST00000279146.7:c.541_542delinsCT ENSP00000279146.3:p.Leu181=
ENST00000525341.1:c.193_194delinsCT ENSP00000476993.1:p.Leu65=
ENST00000528641.6:c.352_353delinsCT ENSP00000434982.2:p.Leu118=
NM_001302959.1:c.364_365delinsCT NP_001289888.1:p.Leu122=
NM_001302960.1:c.541_542delinsCT NP_001289889.1:p.Leu181=
NM_003977.3:c.541_542delinsCT NP_003968.3:p.Leu181=
XM_024448761.1:c.541_542delinsCT XP_024304529.1:p.Leu181=
NM_003977.4:c.541_542delinsCT MANE Select NP_003968.3:p.Leu181=
NM_001302960.2:c.541_542delinsCT NP_001289889.1:p.Leu181=
NM_001302959.2:c.364_365delinsCT NP_001289888.1:p.Leu122=