Canonical Allele Identifier: CA2574896311

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490872_67490877del , CM000673.2:g.67490872_67490877del	GRCh38
NC_000011.9:g.67258343_67258348del , CM000673.1:g.67258343_67258348del	GRCh37
NC_000011.8:g.67014919_67014924del	NCBI36
NG_008969.1:g.12839_12844del , LRG_460:g.12839_12844del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1179_1184del
ENST00000528641.7:c.683_688del	ENSP00000434982.3:p.Val228_Leu229del
ENST00000529797.2:n.1714_1719del
ENST00000682324.1:c.469-125_469-120del	ENSP00000508017.1:n.469-125_469-120del
ENST00000682659.1:c.503_508del	ENSP00000507351.1:p.Val168_Leu169del
ENST00000682699.1:c.872_877del	ENSP00000507935.1:p.Val291_Leu292del
ENST00000683237.1:c.*12_*17del	ENSP00000507343.1:n.*12_*17del
ENST00000683856.1:c.695_700del	ENSP00000507979.1:p.Val232_Leu233del
ENST00000684006.1:c.*12_*17del	ENSP00000507269.1:n.*12_*17del
ENST00000684657.1:c.692_697del	ENSP00000507961.1:p.Val231_Leu232del
ENST00000279146.8:c.872_877del MANE Select	ENSP00000279146.3:p.Val291_Leu292del
ENST00000279146.7:c.872_877del	ENSP00000279146.3:p.Val291_Leu292del
ENST00000528641.6:c.683_688del	ENSP00000434982.2:p.Val228_Leu229del
NM_001302959.1:c.695_700del	NP_001289888.1:p.Val232_Leu233del
NM_001302960.1:c.*12_*17del	NP_001289889.1:n.*12_*17del
NM_003977.3:c.872_877del	NP_003968.3:p.Val291_Leu292del
XM_024448761.1:c.872_877del	XP_024304529.1:p.Val291_Leu292del
NM_003977.4:c.872_877del MANE Select	NP_003968.3:p.Val291_Leu292del
NM_001302960.2:c.*12_*17del	NP_001289889.1:n.*12_*17del
NM_001302959.2:c.695_700del	NP_001289888.1:p.Val232_Leu233del