Canonical Allele Identifier: CA1980172658

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490832G= , CM000673.2:g.67490832G=	GRCh38
NC_000011.9:g.67258303G= , CM000673.1:g.67258303G=	GRCh37
NC_000011.8:g.67014879G=	NCBI36
NG_008969.1:g.12799G= , LRG_460:g.12799G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1139G=
ENST00000528641.7:c.643G=	ENSP00000434982.3:p.Val215=
ENST00000529797.2:n.1674G=
ENST00000682324.1:c.469-165G=	ENSP00000508017.1:n.469-165G=
ENST00000682659.1:c.463G=	ENSP00000507351.1:p.Val155=
ENST00000682699.1:c.832G=	ENSP00000507935.1:p.Val278=
ENST00000683237.1:c.824G=	ENSP00000507343.1:p.Arg275=
ENST00000683856.1:c.655G=	ENSP00000507979.1:p.Val219=
ENST00000684006.1:c.821G=	ENSP00000507269.1:p.Arg274=
ENST00000684657.1:c.652G=	ENSP00000507961.1:p.Val218=
ENST00000279146.8:c.832G= MANE Select	ENSP00000279146.3:p.Val278=
ENST00000279146.7:c.832G=	ENSP00000279146.3:p.Val278=
ENST00000528641.6:c.643G=	ENSP00000434982.2:p.Val215=
NM_001302959.1:c.655G=	NP_001289888.1:p.Val219=
NM_001302960.1:c.824G=	NP_001289889.1:p.Arg275=
NM_003977.3:c.832G=	NP_003968.3:p.Val278=
XM_024448761.1:c.832G=	XP_024304529.1:p.Val278=
NM_003977.4:c.832G= MANE Select	NP_003968.3:p.Val278=
NM_001302960.2:c.824G=	NP_001289889.1:p.Arg275=
NM_001302959.2:c.655G=	NP_001289888.1:p.Val219=