Canonical Allele Identifier: CA1980172695

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490911G= , CM000673.2:g.67490911G=	GRCh38
NC_000011.9:g.67258382G= , CM000673.1:g.67258382G=	GRCh37
NC_000011.8:g.67014958G=	NCBI36
NG_008969.1:g.12878G= , LRG_460:g.12878G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003977.4:c.911G= MANE Select	NP_003968.3:p.Arg304=
ENST00000279146.8:c.911G= MANE Select	ENSP00000279146.3:p.Arg304=
NM_001302959.1:c.734G=	NP_001289888.1:p.Arg245=
NM_001302959.2:c.734G=	NP_001289888.1:p.Arg245=
NM_001302960.1:c.*51G=	NP_001289889.1:n.*51G=
NM_001302960.2:c.*51G=	NP_001289889.1:n.*51G=
NM_003977.3:c.911G=	NP_003968.3:p.Arg304=
ENST00000279146.7:c.911G=	ENSP00000279146.3:p.Arg304=
ENST00000525341.2:c.1218G=
ENST00000528641.7:c.722G=	ENSP00000434982.3:p.Arg241=
ENST00000529797.2:n.1753G=
ENST00000682324.1:c.469-86G=	ENSP00000508017.1:n.469-86G=
ENST00000682659.1:c.542G=	ENSP00000507351.1:p.Arg181=
ENST00000682699.1:c.911G=	ENSP00000507935.1:p.Arg304=
ENST00000683237.1:c.*51G=	ENSP00000507343.1:n.*51G=
ENST00000683856.1:c.734G=	ENSP00000507979.1:p.Arg245=
ENST00000684006.1:c.*51G=	ENSP00000507269.1:n.*51G=
ENST00000684657.1:c.731G=	ENSP00000507961.1:p.Arg244=
XM_024448761.1:c.911G=	XP_024304529.1:p.Arg304=