Canonical Allele Identifier: CA1980172534

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490588_67490589delinsGC , CM000673.2:g.67490588_67490589delinsGC	GRCh38
NC_000011.9:g.67258059_67258060delinsGC , CM000673.1:g.67258059_67258060delinsGC	GRCh37
NC_000011.8:g.67014635_67014636delinsGC	NCBI36
NG_008969.1:g.12555_12556delinsGC , LRG_460:g.12555_12556delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.895_896delinsGC
ENST00000528641.7:c.598+131_598+132delinsGC	ENSP00000434982.3:n.598+131_598+132delinsGC
ENST00000529797.2:n.1430_1431delinsGC
ENST00000682324.1:c.469-409_469-408delinsGC	ENSP00000508017.1:n.469-409_469-408delinsGC
ENST00000682659.1:c.418+131_418+132delinsGC	ENSP00000507351.1:n.418+131_418+132delinsGC
ENST00000682699.1:c.787+131_787+132delinsGC	ENSP00000507935.1:n.787+131_787+132delinsGC
ENST00000683237.1:c.779+139_779+140delinsGC	ENSP00000507343.1:n.779+139_779+140delinsGC
ENST00000683856.1:c.610+131_610+132delinsGC	ENSP00000507979.1:n.610+131_610+132delinsGC
ENST00000684006.1:c.787+131_787+132delinsGC	ENSP00000507269.1:n.787+131_787+132delinsGC
ENST00000684657.1:c.607+131_607+132delinsGC	ENSP00000507961.1:n.607+131_607+132delinsGC
ENST00000279146.8:c.787+131_787+132delinsGC MANE Select	ENSP00000279146.3:n.787+131_787+132delinsGC
ENST00000279146.7:c.787+131_787+132delinsGC	ENSP00000279146.3:n.787+131_787+132delinsGC
ENST00000525341.1:c.570_571delinsGC	ENSP00000476993.1:n.570_571delinsGC
ENST00000528641.6:c.598+131_598+132delinsGC	ENSP00000434982.2:n.598+131_598+132delinsGC
NM_001302959.1:c.610+131_610+132delinsGC	NP_001289888.1:n.610+131_610+132delinsGC
NM_001302960.1:c.779+139_779+140delinsGC	NP_001289889.1:n.779+139_779+140delinsGC
NM_003977.3:c.787+131_787+132delinsGC	NP_003968.3:n.787+131_787+132delinsGC
XM_024448761.1:c.787+131_787+132delinsGC	XP_024304529.1:n.787+131_787+132delinsGC
NM_003977.4:c.787+131_787+132delinsGC MANE Select	NP_003968.3:n.787+131_787+132delinsGC
NM_001302960.2:c.779+139_779+140delinsGC	NP_001289889.1:n.779+139_779+140delinsGC
NM_001302959.2:c.610+131_610+132delinsGC	NP_001289888.1:n.610+131_610+132delinsGC