Canonical Allele Identifier: CA2840623765
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490326_67490327insATCCATTCAGGGGACCCAGGCTGTTCCTGG , CM000673.2:g.67490326_67490327insATCCATTCAGGGGACCCAGGCTGTTCCTGG GRCh38
NC_000011.9:g.67257797_67257798insATCCATTCAGGGGACCCAGGCTGTTCCTGG , CM000673.1:g.67257797_67257798insATCCATTCAGGGGACCCAGGCTGTTCCTGG GRCh37
NC_000011.8:g.67014373_67014374insATCCATTCAGGGGACCCAGGCTGTTCCTGG NCBI36
NG_008969.1:g.12293_12294insATCCATTCAGGGGACCCAGGCTGTTCCTGG , LRG_460:g.12293_12294insATCCATTCAGGGGACCCAGGCTGTTCCTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000525341.2:c.633_634insATCCATTCAGGGGACCCAGGCTGTTCCTGG
ENST00000528641.7:c.467_468insATCCATTCAGGGGACCCAGGCTGTTCCTGG ENSP00000434982.3:p.Gly156_Ser157insSerIleGlnGlyThrGlnAlaValP...
ENST00000529797.2:n.1168_1169insATCCATTCAGGGGACCCAGGCTGTTCCTGG
ENST00000682324.1:c.469-671_469-670insATCCATTCAGGGGACCCAGGCTGTTCCTGG ENSP00000508017.1:n.469-671_469-670insATCCATTCAGGGGACCCAGGCTG...
ENST00000682659.1:c.287_288insATCCATTCAGGGGACCCAGGCTGTTCCTGG ENSP00000507351.1:p.Gly96_Ser97insSerIleGlnGlyThrGlnAlaValPro...
ENST00000682699.1:c.656_657insATCCATTCAGGGGACCCAGGCTGTTCCTGG ENSP00000507935.1:p.Gly219_Ser220insSerIleGlnGlyThrGlnAlaValP...
ENST00000683237.1:c.656_657insATCCATTCAGGGGACCCAGGCTGTTCCTGG ENSP00000507343.1:p.Gly219_Ser220insSerIleGlnGlyThrGlnAlaValP...
ENST00000683856.1:c.479_480insATCCATTCAGGGGACCCAGGCTGTTCCTGG ENSP00000507979.1:p.Gly160_Ser161insSerIleGlnGlyThrGlnAlaValP...
ENST00000684006.1:c.656_657insATCCATTCAGGGGACCCAGGCTGTTCCTGG ENSP00000507269.1:p.Gly219_Ser220insSerIleGlnGlyThrGlnAlaValP...
ENST00000684657.1:c.476_477insATCCATTCAGGGGACCCAGGCTGTTCCTGG ENSP00000507961.1:p.Gly159_Ser160insSerIleGlnGlyThrGlnAlaValP...
ENST00000279146.8:c.656_657insATCCATTCAGGGGACCCAGGCTGTTCCTGG MANE Select ENSP00000279146.3:p.Gly219_Ser220insSerIleGlnGlyThrGlnAlaValP...
ENST00000279146.7:c.656_657insATCCATTCAGGGGACCCAGGCTGTTCCTGG ENSP00000279146.3:p.Gly219_Ser220insSerIleGlnGlyThrGlnAlaValP...
ENST00000525341.1:c.308_309insATCCATTCAGGGGACCCAGGCTGTTCCTGG ENSP00000476993.1:p.Gly103_Ser104insSerIleGlnGlyThrGlnAlaValP...
ENST00000528641.6:c.467_468insATCCATTCAGGGGACCCAGGCTGTTCCTGG ENSP00000434982.2:p.Gly156_Ser157insSerIleGlnGlyThrGlnAlaValP...
NM_001302959.1:c.479_480insATCCATTCAGGGGACCCAGGCTGTTCCTGG NP_001289888.1:p.Gly160_Ser161insSerIleGlnGlyThrGlnAlaValProG...
NM_001302960.1:c.656_657insATCCATTCAGGGGACCCAGGCTGTTCCTGG NP_001289889.1:p.Gly219_Ser220insSerIleGlnGlyThrGlnAlaValProG...
NM_003977.3:c.656_657insATCCATTCAGGGGACCCAGGCTGTTCCTGG NP_003968.3:p.Gly219_Ser220insSerIleGlnGlyThrGlnAlaValProGly
XM_024448761.1:c.656_657insATCCATTCAGGGGACCCAGGCTGTTCCTGG XP_024304529.1:p.Gly219_Ser220insSerIleGlnGlyThrGlnAlaValProG...
NM_003977.4:c.656_657insATCCATTCAGGGGACCCAGGCTGTTCCTGG MANE Select NP_003968.3:p.Gly219_Ser220insSerIleGlnGlyThrGlnAlaValProGly
NM_001302960.2:c.656_657insATCCATTCAGGGGACCCAGGCTGTTCCTGG NP_001289889.1:p.Gly219_Ser220insSerIleGlnGlyThrGlnAlaValProG...
NM_001302959.2:c.479_480insATCCATTCAGGGGACCCAGGCTGTTCCTGG NP_001289888.1:p.Gly160_Ser161insSerIleGlnGlyThrGlnAlaValProG...