Canonical Allele Identifier: CA1980171946

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489332_67489359delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT , CM000673.2:g.67489332_67489359delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT	GRCh38
NC_000011.9:g.67256803_67256830delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT , CM000673.1:g.67256803_67256830delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT	GRCh37
NC_000011.8:g.67013379_67013406delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT	NCBI36
NG_008969.1:g.11299_11326delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT , LRG_460:g.11299_11326delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.322_349delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT
ENST00000528641.7:c.280-706_280-679delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT	ENSP00000434982.3:n.280-706_280-679delins...
ENST00000529797.2:n.275_302delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT
ENST00000682324.1:c.345_372delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT	ENSP00000508017.1:p.Leu115=
ENST00000682659.1:c.100-706_100-679delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT	ENSP00000507351.1:n.100-706_100-679delins...
ENST00000682699.1:c.345_372delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT	ENSP00000507935.1:p.Leu115=
ENST00000683237.1:c.345_372delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT	ENSP00000507343.1:p.Leu115=
ENST00000683856.1:c.168_195delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT	ENSP00000507979.1:p.Leu56=
ENST00000684006.1:c.345_372delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT	ENSP00000507269.1:p.Leu115=
ENST00000684657.1:c.165_192delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT	ENSP00000507961.1:p.Leu55=
ENST00000279146.8:c.345_372delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT MANE Select	ENSP00000279146.3:p.Leu115=
ENST00000279146.7:c.345_372delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT	ENSP00000279146.3:p.Leu115=
ENST00000528641.6:c.280-706_280-679delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT	ENSP00000434982.2:n.280-706_280-679delins...
ENST00000529797.1:n.455_482delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT
NM_001302959.1:c.168_195delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT	NP_001289888.1:p.Leu56=
NM_001302960.1:c.345_372delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT	NP_001289889.1:p.Leu115=
NM_003977.3:c.345_372delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT	NP_003968.3:p.Leu115=
XM_024448761.1:c.345_372delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT	XP_024304529.1:p.Leu115=
NM_003977.4:c.345_372delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT MANE Select	NP_003968.3:p.Leu115=
NM_001302960.2:c.345_372delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT	NP_001289889.1:p.Leu115=
NM_001302959.2:c.168_195delinsGGAGGGCCAGCGGCACTGCTGCGGTGTT	NP_001289888.1:p.Leu56=