Canonical Allele Identifier: CA1980172506

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490515_67490519delinsCCTGT , CM000673.2:g.67490515_67490519delinsCCTGT	GRCh38
NC_000011.9:g.67257986_67257990delinsCCTGT , CM000673.1:g.67257986_67257990delinsCCTGT	GRCh37
NC_000011.8:g.67014562_67014566delinsCCTGT	NCBI36
NG_008969.1:g.12482_12486delinsCCTGT , LRG_460:g.12482_12486delinsCCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.822_826delinsCCTGT
ENST00000528641.7:c.598+58_598+62delinsCCTGT	ENSP00000434982.3:n.598+58_598+62delinsCCTGT
ENST00000529797.2:n.1357_1361delinsCCTGT
ENST00000682324.1:c.469-482_469-478delinsCCTGT	ENSP00000508017.1:n.469-482_469-478delinsCCTGT
ENST00000682659.1:c.418+58_418+62delinsCCTGT	ENSP00000507351.1:n.418+58_418+62delinsCCTGT
ENST00000682699.1:c.787+58_787+62delinsCCTGT	ENSP00000507935.1:n.787+58_787+62delinsCCTGT
ENST00000683237.1:c.779+66_779+70delinsCCTGT	ENSP00000507343.1:n.779+66_779+70delinsCCTGT
ENST00000683856.1:c.610+58_610+62delinsCCTGT	ENSP00000507979.1:n.610+58_610+62delinsCCTGT
ENST00000684006.1:c.787+58_787+62delinsCCTGT	ENSP00000507269.1:n.787+58_787+62delinsCCTGT
ENST00000684657.1:c.607+58_607+62delinsCCTGT	ENSP00000507961.1:n.607+58_607+62delinsCCTGT
ENST00000279146.8:c.787+58_787+62delinsCCTGT MANE Select	ENSP00000279146.3:n.787+58_787+62delinsCCTGT
ENST00000279146.7:c.787+58_787+62delinsCCTGT	ENSP00000279146.3:n.787+58_787+62delinsCCTGT
ENST00000525341.1:c.497_501delinsCCTGT	ENSP00000476993.1:p.Ser166=
ENST00000528641.6:c.598+58_598+62delinsCCTGT	ENSP00000434982.2:n.598+58_598+62delinsCCTGT
NM_001302959.1:c.610+58_610+62delinsCCTGT	NP_001289888.1:n.610+58_610+62delinsCCTGT
NM_001302960.1:c.779+66_779+70delinsCCTGT	NP_001289889.1:n.779+66_779+70delinsCCTGT
NM_003977.3:c.787+58_787+62delinsCCTGT	NP_003968.3:n.787+58_787+62delinsCCTGT
XM_024448761.1:c.787+58_787+62delinsCCTGT	XP_024304529.1:n.787+58_787+62delinsCCTGT
NM_003977.4:c.787+58_787+62delinsCCTGT MANE Select	NP_003968.3:n.787+58_787+62delinsCCTGT
NM_001302960.2:c.779+66_779+70delinsCCTGT	NP_001289889.1:n.779+66_779+70delinsCCTGT
NM_001302959.2:c.610+58_610+62delinsCCTGT	NP_001289888.1:n.610+58_610+62delinsCCTGT