Canonical Allele Identifier: CA1980172675

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490872T= , CM000673.2:g.67490872T=	GRCh38
NC_000011.9:g.67258343T= , CM000673.1:g.67258343T=	GRCh37
NC_000011.8:g.67014919T=	NCBI36
NG_008969.1:g.12839T= , LRG_460:g.12839T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1179T=
ENST00000528641.7:c.683T=	ENSP00000434982.3:p.Val228=
ENST00000529797.2:n.1714T=
ENST00000682324.1:c.469-125T=	ENSP00000508017.1:n.469-125T=
ENST00000682659.1:c.503T=	ENSP00000507351.1:p.Val168=
ENST00000682699.1:c.872T=	ENSP00000507935.1:p.Val291=
ENST00000683237.1:c.*12T=	ENSP00000507343.1:n.*12T=
ENST00000683856.1:c.695T=	ENSP00000507979.1:p.Val232=
ENST00000684006.1:c.*12T=	ENSP00000507269.1:n.*12T=
ENST00000684657.1:c.692T=	ENSP00000507961.1:p.Val231=
ENST00000279146.8:c.872T= MANE Select	ENSP00000279146.3:p.Val291=
ENST00000279146.7:c.872T=	ENSP00000279146.3:p.Val291=
ENST00000528641.6:c.683T=	ENSP00000434982.2:p.Val228=
NM_001302959.1:c.695T=	NP_001289888.1:p.Val232=
NM_001302960.1:c.*12T=	NP_001289889.1:n.*12T=
NM_003977.3:c.872T=	NP_003968.3:p.Val291=
XM_024448761.1:c.872T=	XP_024304529.1:p.Val291=
NM_003977.4:c.872T= MANE Select	NP_003968.3:p.Val291=
NM_001302960.2:c.*12T=	NP_001289889.1:n.*12T=
NM_001302959.2:c.695T=	NP_001289888.1:p.Val232=