Canonical Allele Identifier: CA1980171951

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489342_67489358delinsCGGCACTGCTGCGGTGT , CM000673.2:g.67489342_67489358delinsCGGCACTGCTGCGGTGT	GRCh38
NC_000011.9:g.67256813_67256829delinsCGGCACTGCTGCGGTGT , CM000673.1:g.67256813_67256829delinsCGGCACTGCTGCGGTGT	GRCh37
NC_000011.8:g.67013389_67013405delinsCGGCACTGCTGCGGTGT	NCBI36
NG_008969.1:g.11309_11325delinsCGGCACTGCTGCGGTGT , LRG_460:g.11309_11325delinsCGGCACTGCTGCGGTGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.332_348delinsCGGCACTGCTGCGGTGT
ENST00000528641.7:c.280-696_280-680delinsCGGCACTGCTGCGGTGT	ENSP00000434982.3:n.280-696_280-680delins...
ENST00000529797.2:n.285_301delinsCGGCACTGCTGCGGTGT
ENST00000682324.1:c.355_371delinsCGGCACTGCTGCGGTGT	ENSP00000508017.1:p.Arg119=
ENST00000682659.1:c.100-696_100-680delinsCGGCACTGCTGCGGTGT	ENSP00000507351.1:n.100-696_100-680delins...
ENST00000682699.1:c.355_371delinsCGGCACTGCTGCGGTGT	ENSP00000507935.1:p.Arg119=
ENST00000683237.1:c.355_371delinsCGGCACTGCTGCGGTGT	ENSP00000507343.1:p.Arg119=
ENST00000683856.1:c.178_194delinsCGGCACTGCTGCGGTGT	ENSP00000507979.1:p.Arg60=
ENST00000684006.1:c.355_371delinsCGGCACTGCTGCGGTGT	ENSP00000507269.1:p.Arg119=
ENST00000684657.1:c.175_191delinsCGGCACTGCTGCGGTGT	ENSP00000507961.1:p.Arg59=
ENST00000279146.8:c.355_371delinsCGGCACTGCTGCGGTGT MANE Select	ENSP00000279146.3:p.Arg119=
ENST00000279146.7:c.355_371delinsCGGCACTGCTGCGGTGT	ENSP00000279146.3:p.Arg119=
ENST00000525341.1:c.7_23delinsCGGCACTGCTGCGGTGT	ENSP00000476993.1:p.Arg3=
ENST00000528641.6:c.280-696_280-680delinsCGGCACTGCTGCGGTGT	ENSP00000434982.2:n.280-696_280-680delins...
ENST00000529797.1:n.465_481delinsCGGCACTGCTGCGGTGT
NM_001302959.1:c.178_194delinsCGGCACTGCTGCGGTGT	NP_001289888.1:p.Arg60=
NM_001302960.1:c.355_371delinsCGGCACTGCTGCGGTGT	NP_001289889.1:p.Arg119=
NM_003977.3:c.355_371delinsCGGCACTGCTGCGGTGT	NP_003968.3:p.Arg119=
XM_024448761.1:c.355_371delinsCGGCACTGCTGCGGTGT	XP_024304529.1:p.Arg119=
NM_003977.4:c.355_371delinsCGGCACTGCTGCGGTGT MANE Select	NP_003968.3:p.Arg119=
NM_001302960.2:c.355_371delinsCGGCACTGCTGCGGTGT	NP_001289889.1:p.Arg119=
NM_001302959.2:c.178_194delinsCGGCACTGCTGCGGTGT	NP_001289888.1:p.Arg60=