Canonical Allele Identifier: CA2614621756

Gene: AIP

Linked Data

• gnomAD v4: 11-67489570-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489574_67489575del , CM000673.2:g.67489574_67489575del	GRCh38
NC_000011.9:g.67257045_67257046del , CM000673.1:g.67257045_67257046del	GRCh37
NC_000011.8:g.67013621_67013622del	NCBI36
NG_008969.1:g.11541_11542del , LRG_460:g.11541_11542del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.445+119_445+120del
ENST00000528641.7:c.280-464_280-463del	ENSP00000434982.3:n.280-464_280-463del
ENST00000529797.2:n.517_518del
ENST00000682324.1:c.468+119_468+120del	ENSP00000508017.1:n.468+119_468+120del
ENST00000682659.1:c.100-464_100-463del	ENSP00000507351.1:n.100-464_100-463del
ENST00000682699.1:c.468+119_468+120del	ENSP00000507935.1:n.468+119_468+120del
ENST00000683237.1:c.468+119_468+120del	ENSP00000507343.1:n.468+119_468+120del
ENST00000683856.1:c.291+119_291+120del	ENSP00000507979.1:n.291+119_291+120del
ENST00000684006.1:c.468+119_468+120del	ENSP00000507269.1:n.468+119_468+120del
ENST00000684657.1:c.288+119_288+120del	ENSP00000507961.1:n.288+119_288+120del
ENST00000279146.8:c.468+119_468+120del MANE Select	ENSP00000279146.3:n.468+119_468+120del
ENST00000279146.7:c.468+119_468+120del	ENSP00000279146.3:n.468+119_468+120del
ENST00000525341.1:c.120+119_120+120del	ENSP00000476993.1:n.120+119_120+120del
ENST00000528641.6:c.280-464_280-463del	ENSP00000434982.2:n.280-464_280-463del
ENST00000529797.1:n.697_698del
NM_001302959.1:c.291+119_291+120del	NP_001289888.1:n.291+119_291+120del
NM_001302960.1:c.468+119_468+120del	NP_001289889.1:n.468+119_468+120del
NM_003977.3:c.468+119_468+120del	NP_003968.3:n.468+119_468+120del
XM_024448761.1:c.468+119_468+120del	XP_024304529.1:n.468+119_468+120del
NM_003977.4:c.468+119_468+120del MANE Select	NP_003968.3:n.468+119_468+120del
NM_001302960.2:c.468+119_468+120del	NP_001289889.1:n.468+119_468+120del
NM_001302959.2:c.291+119_291+120del	NP_001289888.1:n.291+119_291+120del