Canonical Allele Identifier: CA2580610711

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490176_67490177dup , CM000673.2:g.67490176_67490177dup	GRCh38
NC_000011.9:g.67257647_67257648dup , CM000673.1:g.67257647_67257648dup	GRCh37
NC_000011.8:g.67014223_67014224dup	NCBI36
NG_008969.1:g.12143_12144dup , LRG_460:g.12143_12144dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.584_585dup
ENST00000528641.7:c.418_419dup	ENSP00000434982.3:p.Asp141ThrfsTer12
ENST00000529797.2:n.1119_1120dup
ENST00000682324.1:c.468+721_468+722dup	ENSP00000508017.1:n.468+721_468+722dup
ENST00000682659.1:c.238_239dup	ENSP00000507351.1:p.Asp81ThrfsTer12
ENST00000682699.1:c.607_608dup	ENSP00000507935.1:p.Asp204ThrfsTer12
ENST00000683237.1:c.607_608dup	ENSP00000507343.1:p.Asp204ThrfsTer12
ENST00000683856.1:c.430_431dup	ENSP00000507979.1:p.Asp145ThrfsTer12
ENST00000684006.1:c.607_608dup	ENSP00000507269.1:p.Asp204ThrfsTer12
ENST00000684657.1:c.427_428dup	ENSP00000507961.1:p.Asp144ThrfsTer12
ENST00000279146.8:c.607_608dup MANE Select	ENSP00000279146.3:p.Asp204ThrfsTer12
ENST00000279146.7:c.607_608dup	ENSP00000279146.3:p.Asp204ThrfsTer12
ENST00000525341.1:c.259_260dup	ENSP00000476993.1:p.Asp88ThrfsTer12
ENST00000528641.6:c.418_419dup	ENSP00000434982.2:p.Asp141ThrfsTer12
NM_001302959.1:c.430_431dup	NP_001289888.1:p.Asp145ThrfsTer12
NM_001302960.1:c.607_608dup	NP_001289889.1:p.Asp204ThrfsTer12
NM_003977.3:c.607_608dup	NP_003968.3:p.Asp204ThrfsTer12
XM_024448761.1:c.607_608dup	XP_024304529.1:p.Asp204ThrfsTer12
NM_003977.4:c.607_608dup MANE Select	NP_003968.3:p.Asp204ThrfsTer12
NM_001302960.2:c.607_608dup	NP_001289889.1:p.Asp204ThrfsTer12
NM_001302959.2:c.430_431dup	NP_001289888.1:p.Asp145ThrfsTer12