Canonical Allele Identifier: CA2614624463

Gene: AIP

Linked Data

• gnomAD v4: 11-67490476-G-GCTGCAGCAGCTCATTTCCTTTATAGCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490480_67490481insAGCAGCTCATTTCCTTTATAGCCTCTGC , CM000673.2:g.67490480_67490481insAGCAGCTCATTTCCTTTATAGCCTCTGC	GRCh38
NC_000011.9:g.67257951_67257952insAGCAGCTCATTTCCTTTATAGCCTCTGC , CM000673.1:g.67257951_67257952insAGCAGCTCATTTCCTTTATAGCCTCTGC	GRCh37
NC_000011.8:g.67014527_67014528insAGCAGCTCATTTCCTTTATAGCCTCTGC	NCBI36
NG_008969.1:g.12447_12448insAGCAGCTCATTTCCTTTATAGCCTCTGC , LRG_460:g.12447_12448insAGCAGCTCATTTCCTTTATAGCCTCTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.787_788insAGCAGCTCATTTCCTTTATAGCCTCTGC
ENST00000528641.7:c.598+23_598+24insAGCAGCTCATTTCCTTTATAGCCTCTGC	ENSP00000434982.3:n.598+23_598+24insAGCAGCTCATTTCCTTTATAGCCTC...
ENST00000529797.2:n.1322_1323insAGCAGCTCATTTCCTTTATAGCCTCTGC
ENST00000682324.1:c.469-517_469-516insAGCAGCTCATTTCCTTTATAGCCTCTGC	ENSP00000508017.1:n.469-517_469-516insAGCAGCTCATTTCCTTTATAGCC...
ENST00000682659.1:c.418+23_418+24insAGCAGCTCATTTCCTTTATAGCCTCTGC	ENSP00000507351.1:n.418+23_418+24insAGCAGCTCATTTCCTTTATAGCCTC...
ENST00000682699.1:c.787+23_787+24insAGCAGCTCATTTCCTTTATAGCCTCTGC	ENSP00000507935.1:n.787+23_787+24insAGCAGCTCATTTCCTTTATAGCCTC...
ENST00000683237.1:c.779+31_779+32insAGCAGCTCATTTCCTTTATAGCCTCTGC	ENSP00000507343.1:n.779+31_779+32insAGCAGCTCATTTCCTTTATAGCCTC...
ENST00000683856.1:c.610+23_610+24insAGCAGCTCATTTCCTTTATAGCCTCTGC	ENSP00000507979.1:n.610+23_610+24insAGCAGCTCATTTCCTTTATAGCCTC...
ENST00000684006.1:c.787+23_787+24insAGCAGCTCATTTCCTTTATAGCCTCTGC	ENSP00000507269.1:n.787+23_787+24insAGCAGCTCATTTCCTTTATAGCCTC...
ENST00000684657.1:c.607+23_607+24insAGCAGCTCATTTCCTTTATAGCCTCTGC	ENSP00000507961.1:n.607+23_607+24insAGCAGCTCATTTCCTTTATAGCCTC...
ENST00000279146.8:c.787+23_787+24insAGCAGCTCATTTCCTTTATAGCCTCTGC MANE Select	ENSP00000279146.3:n.787+23_787+24insAGCAGCTCATTTCCTTTATAGCCTC...
ENST00000279146.7:c.787+23_787+24insAGCAGCTCATTTCCTTTATAGCCTCTGC	ENSP00000279146.3:n.787+23_787+24insAGCAGCTCATTTCCTTTATAGCCTC...
ENST00000525341.1:c.462_463insAGCAGCTCATTTCCTTTATAGCCTCTGC	ENSP00000476993.1:p.Arg155SerfsTer7
ENST00000528641.6:c.598+23_598+24insAGCAGCTCATTTCCTTTATAGCCTCTGC	ENSP00000434982.2:n.598+23_598+24insAGCAGCTCATTTCCTTTATAGCCTC...
NM_001302959.1:c.610+23_610+24insAGCAGCTCATTTCCTTTATAGCCTCTGC	NP_001289888.1:n.610+23_610+24insAGCAGCTCATTTCCTTTATAGCCTCTGC...
NM_001302960.1:c.779+31_779+32insAGCAGCTCATTTCCTTTATAGCCTCTGC	NP_001289889.1:n.779+31_779+32insAGCAGCTCATTTCCTTTATAGCCTCTGC...
NM_003977.3:c.787+23_787+24insAGCAGCTCATTTCCTTTATAGCCTCTGC	NP_003968.3:n.787+23_787+24insAGCAGCTCATTTCCTTTATAGCCTCTGC
XM_024448761.1:c.787+23_787+24insAGCAGCTCATTTCCTTTATAGCCTCTGC	XP_024304529.1:n.787+23_787+24insAGCAGCTCATTTCCTTTATAGCCTCTGC...
NM_003977.4:c.787+23_787+24insAGCAGCTCATTTCCTTTATAGCCTCTGC MANE Select	NP_003968.3:n.787+23_787+24insAGCAGCTCATTTCCTTTATAGCCTCTGC
NM_001302960.2:c.779+31_779+32insAGCAGCTCATTTCCTTTATAGCCTCTGC	NP_001289889.1:n.779+31_779+32insAGCAGCTCATTTCCTTTATAGCCTCTGC...
NM_001302959.2:c.610+23_610+24insAGCAGCTCATTTCCTTTATAGCCTCTGC	NP_001289888.1:n.610+23_610+24insAGCAGCTCATTTCCTTTATAGCCTCTGC...