Canonical Allele Identifier: CA1980172677

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490878_67490879delinsAG , CM000673.2:g.67490878_67490879delinsAG	GRCh38
NC_000011.9:g.67258349_67258350delinsAG , CM000673.1:g.67258349_67258350delinsAG	GRCh37
NC_000011.8:g.67014925_67014926delinsAG	NCBI36
NG_008969.1:g.12845_12846delinsAG , LRG_460:g.12845_12846delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1185_1186delinsAG
ENST00000528641.7:c.689_690delinsAG	ENSP00000434982.3:p.Glu230=
ENST00000529797.2:n.1720_1721delinsAG
ENST00000682324.1:c.469-119_469-118delinsAG	ENSP00000508017.1:n.469-119_469-118delinsAG
ENST00000682659.1:c.509_510delinsAG	ENSP00000507351.1:p.Glu170=
ENST00000682699.1:c.878_879delinsAG	ENSP00000507935.1:p.Glu293=
ENST00000683237.1:c.*18_*19delinsAG	ENSP00000507343.1:n.*18_*19delinsAG
ENST00000683856.1:c.701_702delinsAG	ENSP00000507979.1:p.Glu234=
ENST00000684006.1:c.*18_*19delinsAG	ENSP00000507269.1:n.*18_*19delinsAG
ENST00000684657.1:c.698_699delinsAG	ENSP00000507961.1:p.Glu233=
ENST00000279146.8:c.878_879delinsAG MANE Select	ENSP00000279146.3:p.Glu293=
ENST00000279146.7:c.878_879delinsAG	ENSP00000279146.3:p.Glu293=
ENST00000528641.6:c.689_690delinsAG	ENSP00000434982.2:p.Glu230=
NM_001302959.1:c.701_702delinsAG	NP_001289888.1:p.Glu234=
NM_001302960.1:c.*18_*19delinsAG	NP_001289889.1:n.*18_*19delinsAG
NM_003977.3:c.878_879delinsAG	NP_003968.3:p.Glu293=
XM_024448761.1:c.878_879delinsAG	XP_024304529.1:p.Glu293=
NM_003977.4:c.878_879delinsAG MANE Select	NP_003968.3:p.Glu293=
NM_001302960.2:c.*18_*19delinsAG	NP_001289889.1:n.*18_*19delinsAG
NM_001302959.2:c.701_702delinsAG	NP_001289888.1:p.Glu234=