Canonical Allele Identifier: CA1980172586

Gene: AIP

Linked Data

• dbSNP Id: rs1308246481
• gnomAD v4: 11-67490678-GCTCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490684_67490687del , CM000673.2:g.67490684_67490687del	GRCh38
NC_000011.9:g.67258155_67258158del , CM000673.1:g.67258155_67258158del	GRCh37
NC_000011.8:g.67014731_67014734del	NCBI36
NG_008969.1:g.12651_12654del , LRG_460:g.12651_12654del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.991_994del
ENST00000528641.7:c.599-104_599-101del	ENSP00000434982.3:n.599-104_599-101del
ENST00000529797.2:n.1526_1529del
ENST00000682324.1:c.469-313_469-310del	ENSP00000508017.1:n.469-313_469-310del
ENST00000682659.1:c.419-104_419-101del	ENSP00000507351.1:n.419-104_419-101del
ENST00000682699.1:c.788-104_788-101del	ENSP00000507935.1:n.788-104_788-101del
ENST00000683237.1:c.780-104_780-101del	ENSP00000507343.1:n.780-104_780-101del
ENST00000683856.1:c.611-104_611-101del	ENSP00000507979.1:n.611-104_611-101del
ENST00000684006.1:c.788-115_788-112del	ENSP00000507269.1:n.788-115_788-112del
ENST00000684657.1:c.608-104_608-101del	ENSP00000507961.1:n.608-104_608-101del
ENST00000279146.8:c.788-104_788-101del MANE Select	ENSP00000279146.3:n.788-104_788-101del
ENST00000279146.7:c.788-104_788-101del	ENSP00000279146.3:n.788-104_788-101del
ENST00000528641.6:c.599-104_599-101del	ENSP00000434982.2:n.599-104_599-101del
NM_001302959.1:c.611-104_611-101del	NP_001289888.1:n.611-104_611-101del
NM_001302960.1:c.780-104_780-101del	NP_001289889.1:n.780-104_780-101del
NM_003977.3:c.788-104_788-101del	NP_003968.3:n.788-104_788-101del
XM_024448761.1:c.788-104_788-101del	XP_024304529.1:n.788-104_788-101del
NM_003977.4:c.788-104_788-101del MANE Select	NP_003968.3:n.788-104_788-101del
NM_001302960.2:c.780-104_780-101del	NP_001289889.1:n.780-104_780-101del
NM_001302959.2:c.611-104_611-101del	NP_001289888.1:n.611-104_611-101del