Canonical Allele Identifier: CA2614621603

Gene: AIP

Linked Data

• gnomAD v4: 11-67489517-GCCTGTCCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489520_67489527del , CM000673.2:g.67489520_67489527del	GRCh38
NC_000011.9:g.67256991_67256998del , CM000673.1:g.67256991_67256998del	GRCh37
NC_000011.8:g.67013567_67013574del	NCBI36
NG_008969.1:g.11487_11494del , LRG_460:g.11487_11494del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.445+65_445+72del
ENST00000528641.7:c.280-518_280-511del	ENSP00000434982.3:n.280-518_280-511del
ENST00000529797.2:n.463_470del
ENST00000682324.1:c.468+65_468+72del	ENSP00000508017.1:n.468+65_468+72del
ENST00000682659.1:c.100-518_100-511del	ENSP00000507351.1:n.100-518_100-511del
ENST00000682699.1:c.468+65_468+72del	ENSP00000507935.1:n.468+65_468+72del
ENST00000683237.1:c.468+65_468+72del	ENSP00000507343.1:n.468+65_468+72del
ENST00000683856.1:c.291+65_291+72del	ENSP00000507979.1:n.291+65_291+72del
ENST00000684006.1:c.468+65_468+72del	ENSP00000507269.1:n.468+65_468+72del
ENST00000684657.1:c.288+65_288+72del	ENSP00000507961.1:n.288+65_288+72del
ENST00000279146.8:c.468+65_468+72del MANE Select	ENSP00000279146.3:n.468+65_468+72del
ENST00000279146.7:c.468+65_468+72del	ENSP00000279146.3:n.468+65_468+72del
ENST00000525341.1:c.120+65_120+72del	ENSP00000476993.1:n.120+65_120+72del
ENST00000528641.6:c.280-518_280-511del	ENSP00000434982.2:n.280-518_280-511del
ENST00000529797.1:n.643_650del
NM_001302959.1:c.291+65_291+72del	NP_001289888.1:n.291+65_291+72del
NM_001302960.1:c.468+65_468+72del	NP_001289889.1:n.468+65_468+72del
NM_003977.3:c.468+65_468+72del	NP_003968.3:n.468+65_468+72del
XM_024448761.1:c.468+65_468+72del	XP_024304529.1:n.468+65_468+72del
NM_003977.4:c.468+65_468+72del MANE Select	NP_003968.3:n.468+65_468+72del
NM_001302960.2:c.468+65_468+72del	NP_001289889.1:n.468+65_468+72del
NM_001302959.2:c.291+65_291+72del	NP_001289888.1:n.291+65_291+72del