Canonical Allele Identifier: CA1980172585

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490678_67490682delinsGCTCT , CM000673.2:g.67490678_67490682delinsGCTCT	GRCh38
NC_000011.9:g.67258149_67258153delinsGCTCT , CM000673.1:g.67258149_67258153delinsGCTCT	GRCh37
NC_000011.8:g.67014725_67014729delinsGCTCT	NCBI36
NG_008969.1:g.12645_12649delinsGCTCT , LRG_460:g.12645_12649delinsGCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.985_989delinsGCTCT
ENST00000528641.7:c.599-110_599-106delinsGCTCT	ENSP00000434982.3:n.599-110_599-106delinsGCTCT
ENST00000529797.2:n.1520_1524delinsGCTCT
ENST00000682324.1:c.469-319_469-315delinsGCTCT	ENSP00000508017.1:n.469-319_469-315delinsGCTCT
ENST00000682659.1:c.419-110_419-106delinsGCTCT	ENSP00000507351.1:n.419-110_419-106delinsGCTCT
ENST00000682699.1:c.788-110_788-106delinsGCTCT	ENSP00000507935.1:n.788-110_788-106delinsGCTCT
ENST00000683237.1:c.780-110_780-106delinsGCTCT	ENSP00000507343.1:n.780-110_780-106delinsGCTCT
ENST00000683856.1:c.611-110_611-106delinsGCTCT	ENSP00000507979.1:n.611-110_611-106delinsGCTCT
ENST00000684006.1:c.788-121_788-117delinsGCTCT	ENSP00000507269.1:n.788-121_788-117delinsGCTCT
ENST00000684657.1:c.608-110_608-106delinsGCTCT	ENSP00000507961.1:n.608-110_608-106delinsGCTCT
ENST00000279146.8:c.788-110_788-106delinsGCTCT MANE Select	ENSP00000279146.3:n.788-110_788-106delinsGCTCT
ENST00000279146.7:c.788-110_788-106delinsGCTCT	ENSP00000279146.3:n.788-110_788-106delinsGCTCT
ENST00000528641.6:c.599-110_599-106delinsGCTCT	ENSP00000434982.2:n.599-110_599-106delinsGCTCT
NM_001302959.1:c.611-110_611-106delinsGCTCT	NP_001289888.1:n.611-110_611-106delinsGCTCT
NM_001302960.1:c.780-110_780-106delinsGCTCT	NP_001289889.1:n.780-110_780-106delinsGCTCT
NM_003977.3:c.788-110_788-106delinsGCTCT	NP_003968.3:n.788-110_788-106delinsGCTCT
XM_024448761.1:c.788-110_788-106delinsGCTCT	XP_024304529.1:n.788-110_788-106delinsGCTCT
NM_003977.4:c.788-110_788-106delinsGCTCT MANE Select	NP_003968.3:n.788-110_788-106delinsGCTCT
NM_001302960.2:c.780-110_780-106delinsGCTCT	NP_001289889.1:n.780-110_780-106delinsGCTCT
NM_001302959.2:c.611-110_611-106delinsGCTCT	NP_001289888.1:n.611-110_611-106delinsGCTCT