Canonical Allele Identifier: CA1980172645

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490811C= , CM000673.2:g.67490811C=	GRCh38
NC_000011.9:g.67258282C= , CM000673.1:g.67258282C=	GRCh37
NC_000011.8:g.67014858C=	NCBI36
NG_008969.1:g.12778C= , LRG_460:g.12778C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1118C=
ENST00000528641.7:c.622C=	ENSP00000434982.3:p.Arg208=
ENST00000529797.2:n.1653C=
ENST00000682324.1:c.469-186C=	ENSP00000508017.1:n.469-186C=
ENST00000682659.1:c.442C=	ENSP00000507351.1:p.Arg148=
ENST00000682699.1:c.811C=	ENSP00000507935.1:p.Arg271=
ENST00000683237.1:c.803C=	ENSP00000507343.1:p.Ala268=
ENST00000683856.1:c.634C=	ENSP00000507979.1:p.Arg212=
ENST00000684006.1:c.800C=	ENSP00000507269.1:p.Ala267=
ENST00000684657.1:c.631C=	ENSP00000507961.1:p.Arg211=
ENST00000279146.8:c.811C= MANE Select	ENSP00000279146.3:p.Arg271=
ENST00000279146.7:c.811C=	ENSP00000279146.3:p.Arg271=
ENST00000528641.6:c.622C=	ENSP00000434982.2:p.Arg208=
NM_001302959.1:c.634C=	NP_001289888.1:p.Arg212=
NM_001302960.1:c.803C=	NP_001289889.1:p.Ala268=
NM_003977.3:c.811C=	NP_003968.3:p.Arg271=
XM_024448761.1:c.811C=	XP_024304529.1:p.Arg271=
NM_003977.4:c.811C= MANE Select	NP_003968.3:p.Arg271=
NM_001302960.2:c.803C=	NP_001289889.1:p.Ala268=
NM_001302959.2:c.634C=	NP_001289888.1:p.Arg212=