Canonical Allele Identifier: CA2614623406

Gene: AIP

Linked Data

• gnomAD v4: 11-67490204-TGCAGATGAAGGTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490205_67490217del , CM000673.2:g.67490205_67490217del	GRCh38
NC_000011.9:g.67257676_67257688del , CM000673.1:g.67257676_67257688del	GRCh37
NC_000011.8:g.67014252_67014264del	NCBI36
NG_008969.1:g.12172_12184del , LRG_460:g.12172_12184del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.613_622+3del
ENST00000528641.7:c.447_456+3del
ENST00000529797.2:n.1148_1157+3del
ENST00000682324.1:c.468+750_468+762del	ENSP00000508017.1:n.468+750_468+762del
ENST00000682659.1:c.267_276+3del
ENST00000682699.1:c.636_645+3del
ENST00000683237.1:c.636_645+3del
ENST00000683856.1:c.459_468+3del
ENST00000684006.1:c.636_645+3del
ENST00000684657.1:c.456_465+3del
ENST00000279146.8:c.636_645+3del
ENST00000279146.7:c.636_645+3del
ENST00000525341.1:c.288_297+3del
ENST00000528641.6:c.447_456+3del
NM_001302959.1:c.459_468+3del
NM_001302960.1:c.636_645+3del
NM_003977.3:c.636_645+3del
XM_024448761.1:c.636_645+3del
NM_003977.4:c.636_645+3del
NM_001302960.2:c.636_645+3del
NM_001302959.2:c.459_468+3del