Canonical Allele Identifier: CA1980172319

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490144A= , CM000673.2:g.67490144A=	GRCh38
NC_000011.9:g.67257615A= , CM000673.1:g.67257615A=	GRCh37
NC_000011.8:g.67014191A=	NCBI36
NG_008969.1:g.12111A= , LRG_460:g.12111A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.552A=
ENST00000528641.7:c.386A=	ENSP00000434982.3:p.Glu129=
ENST00000529797.2:n.1087A=
ENST00000682324.1:c.468+689A=	ENSP00000508017.1:n.468+689A=
ENST00000682659.1:c.206A=	ENSP00000507351.1:p.Glu69=
ENST00000682699.1:c.575A=	ENSP00000507935.1:p.Glu192=
ENST00000683237.1:c.575A=	ENSP00000507343.1:p.Glu192=
ENST00000683856.1:c.398A=	ENSP00000507979.1:p.Glu133=
ENST00000684006.1:c.575A=	ENSP00000507269.1:p.Glu192=
ENST00000684657.1:c.395A=	ENSP00000507961.1:p.Glu132=
ENST00000279146.8:c.575A= MANE Select	ENSP00000279146.3:p.Glu192=
ENST00000279146.7:c.575A=	ENSP00000279146.3:p.Glu192=
ENST00000525341.1:c.227A=	ENSP00000476993.1:p.Glu76=
ENST00000528641.6:c.386A=	ENSP00000434982.2:p.Glu129=
NM_001302959.1:c.398A=	NP_001289888.1:p.Glu133=
NM_001302960.1:c.575A=	NP_001289889.1:p.Glu192=
NM_003977.3:c.575A=	NP_003968.3:p.Glu192=
XM_024448761.1:c.575A=	XP_024304529.1:p.Glu192=
NM_003977.4:c.575A= MANE Select	NP_003968.3:p.Glu192=
NM_001302960.2:c.575A=	NP_001289889.1:p.Glu192=
NM_001302959.2:c.398A=	NP_001289888.1:p.Glu133=