Canonical Allele Identifier: CA1980172593

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490689_67490691delinsCCT , CM000673.2:g.67490689_67490691delinsCCT	GRCh38
NC_000011.9:g.67258160_67258162delinsCCT , CM000673.1:g.67258160_67258162delinsCCT	GRCh37
NC_000011.8:g.67014736_67014738delinsCCT	NCBI36
NG_008969.1:g.12656_12658delinsCCT , LRG_460:g.12656_12658delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.996_998delinsCCT
ENST00000528641.7:c.599-99_599-97delinsCCT	ENSP00000434982.3:n.599-99_599-97delinsCCT
ENST00000529797.2:n.1531_1533delinsCCT
ENST00000682324.1:c.469-308_469-306delinsCCT	ENSP00000508017.1:n.469-308_469-306delinsCCT
ENST00000682659.1:c.419-99_419-97delinsCCT	ENSP00000507351.1:n.419-99_419-97delinsCCT
ENST00000682699.1:c.788-99_788-97delinsCCT	ENSP00000507935.1:n.788-99_788-97delinsCCT
ENST00000683237.1:c.780-99_780-97delinsCCT	ENSP00000507343.1:n.780-99_780-97delinsCCT
ENST00000683856.1:c.611-99_611-97delinsCCT	ENSP00000507979.1:n.611-99_611-97delinsCCT
ENST00000684006.1:c.788-110_788-108delinsCCT	ENSP00000507269.1:n.788-110_788-108delinsCCT
ENST00000684657.1:c.608-99_608-97delinsCCT	ENSP00000507961.1:n.608-99_608-97delinsCCT
ENST00000279146.8:c.788-99_788-97delinsCCT MANE Select	ENSP00000279146.3:n.788-99_788-97delinsCCT
ENST00000279146.7:c.788-99_788-97delinsCCT	ENSP00000279146.3:n.788-99_788-97delinsCCT
ENST00000528641.6:c.599-99_599-97delinsCCT	ENSP00000434982.2:n.599-99_599-97delinsCCT
NM_001302959.1:c.611-99_611-97delinsCCT	NP_001289888.1:n.611-99_611-97delinsCCT
NM_001302960.1:c.780-99_780-97delinsCCT	NP_001289889.1:n.780-99_780-97delinsCCT
NM_003977.3:c.788-99_788-97delinsCCT	NP_003968.3:n.788-99_788-97delinsCCT
XM_024448761.1:c.788-99_788-97delinsCCT	XP_024304529.1:n.788-99_788-97delinsCCT
NM_003977.4:c.788-99_788-97delinsCCT MANE Select	NP_003968.3:n.788-99_788-97delinsCCT
NM_001302960.2:c.780-99_780-97delinsCCT	NP_001289889.1:n.780-99_780-97delinsCCT
NM_001302959.2:c.611-99_611-97delinsCCT	NP_001289888.1:n.611-99_611-97delinsCCT