Canonical Allele Identifier: CA1980172288

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490085_67490090delinsCGAAGA , CM000673.2:g.67490085_67490090delinsCGAAGA	GRCh38
NC_000011.9:g.67257556_67257561delinsCGAAGA , CM000673.1:g.67257556_67257561delinsCGAAGA	GRCh37
NC_000011.8:g.67014132_67014137delinsCGAAGA	NCBI36
NG_008969.1:g.12052_12057delinsCGAAGA , LRG_460:g.12052_12057delinsCGAAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.493_498delinsCGAAGA
ENST00000528641.7:c.327_332delinsCGAAGA	ENSP00000434982.3:p.Asp109=
ENST00000529797.2:n.1028_1033delinsCGAAGA
ENST00000682324.1:c.468+630_468+635delinsCGAAGA	ENSP00000508017.1:n.468+630_468+635delinsCGAAGA
ENST00000682659.1:c.147_152delinsCGAAGA	ENSP00000507351.1:p.Asp49=
ENST00000682699.1:c.516_521delinsCGAAGA	ENSP00000507935.1:p.Asp172=
ENST00000683237.1:c.516_521delinsCGAAGA	ENSP00000507343.1:p.Asp172=
ENST00000683856.1:c.339_344delinsCGAAGA	ENSP00000507979.1:p.Asp113=
ENST00000684006.1:c.516_521delinsCGAAGA	ENSP00000507269.1:p.Asp172=
ENST00000684657.1:c.336_341delinsCGAAGA	ENSP00000507961.1:p.Asp112=
ENST00000279146.8:c.516_521delinsCGAAGA MANE Select	ENSP00000279146.3:p.Asp172=
ENST00000279146.7:c.516_521delinsCGAAGA	ENSP00000279146.3:p.Asp172=
ENST00000525341.1:c.168_173delinsCGAAGA	ENSP00000476993.1:p.Asp56=
ENST00000528641.6:c.327_332delinsCGAAGA	ENSP00000434982.2:p.Asp109=
NM_001302959.1:c.339_344delinsCGAAGA	NP_001289888.1:p.Asp113=
NM_001302960.1:c.516_521delinsCGAAGA	NP_001289889.1:p.Asp172=
NM_003977.3:c.516_521delinsCGAAGA	NP_003968.3:p.Asp172=
XM_024448761.1:c.516_521delinsCGAAGA	XP_024304529.1:p.Asp172=
NM_003977.4:c.516_521delinsCGAAGA MANE Select	NP_003968.3:p.Asp172=
NM_001302960.2:c.516_521delinsCGAAGA	NP_001289889.1:p.Asp172=
NM_001302959.2:c.339_344delinsCGAAGA	NP_001289888.1:p.Asp113=