Canonical Allele Identifier: CA2840623728

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489444_67489447del , CM000673.2:g.67489444_67489447del	GRCh38
NC_000011.9:g.67256915_67256918del , CM000673.1:g.67256915_67256918del	GRCh37
NC_000011.8:g.67013491_67013494del	NCBI36
NG_008969.1:g.11411_11414del , LRG_460:g.11411_11414del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.434_437del
ENST00000528641.7:c.280-594_280-591del	ENSP00000434982.3:n.280-594_280-591del
ENST00000529797.2:n.387_390del
ENST00000682324.1:c.457_460del	ENSP00000508017.1:p.Glu153CysfsTer2
ENST00000682659.1:c.100-594_100-591del	ENSP00000507351.1:n.100-594_100-591del
ENST00000682699.1:c.457_460del	ENSP00000507935.1:p.Glu153CysfsTer2
ENST00000683237.1:c.457_460del	ENSP00000507343.1:p.Glu153CysfsTer2
ENST00000683856.1:c.280_283del	ENSP00000507979.1:p.Glu94CysfsTer2
ENST00000684006.1:c.457_460del	ENSP00000507269.1:p.Glu153CysfsTer2
ENST00000684657.1:c.277_280del	ENSP00000507961.1:p.Glu93CysfsTer2
ENST00000279146.8:c.457_460del MANE Select	ENSP00000279146.3:p.Glu153CysfsTer2
ENST00000279146.7:c.457_460del	ENSP00000279146.3:p.Glu153CysfsTer2
ENST00000525341.1:c.109_112del	ENSP00000476993.1:p.Glu37CysfsTer2
ENST00000528641.6:c.280-594_280-591del	ENSP00000434982.2:n.280-594_280-591del
ENST00000529797.1:n.567_570del
NM_001302959.1:c.280_283del	NP_001289888.1:p.Glu94CysfsTer2
NM_001302960.1:c.457_460del	NP_001289889.1:p.Glu153CysfsTer2
NM_003977.3:c.457_460del	NP_003968.3:p.Glu153CysfsTer2
XM_024448761.1:c.457_460del	XP_024304529.1:p.Glu153CysfsTer2
NM_003977.4:c.457_460del MANE Select	NP_003968.3:p.Glu153CysfsTer2
NM_001302960.2:c.457_460del	NP_001289889.1:p.Glu153CysfsTer2
NM_001302959.2:c.280_283del	NP_001289888.1:p.Glu94CysfsTer2