Canonical Allele Identifier: CA1980172286

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490083G= , CM000673.2:g.67490083G=	GRCh38
NC_000011.9:g.67257554G= , CM000673.1:g.67257554G=	GRCh37
NC_000011.8:g.67014130G=	NCBI36
NG_008969.1:g.12050G= , LRG_460:g.12050G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.491G=
ENST00000528641.7:c.325G=	ENSP00000434982.3:p.Asp109=
ENST00000529797.2:n.1026G=
ENST00000682324.1:c.468+628G=	ENSP00000508017.1:n.468+628G=
ENST00000682659.1:c.145G=	ENSP00000507351.1:p.Asp49=
ENST00000682699.1:c.514G=	ENSP00000507935.1:p.Asp172=
ENST00000683237.1:c.514G=	ENSP00000507343.1:p.Asp172=
ENST00000683856.1:c.337G=	ENSP00000507979.1:p.Asp113=
ENST00000684006.1:c.514G=	ENSP00000507269.1:p.Asp172=
ENST00000684657.1:c.334G=	ENSP00000507961.1:p.Asp112=
ENST00000279146.8:c.514G= MANE Select	ENSP00000279146.3:p.Asp172=
ENST00000279146.7:c.514G=	ENSP00000279146.3:p.Asp172=
ENST00000525341.1:c.166G=	ENSP00000476993.1:p.Asp56=
ENST00000528641.6:c.325G=	ENSP00000434982.2:p.Asp109=
NM_001302959.1:c.337G=	NP_001289888.1:p.Asp113=
NM_001302960.1:c.514G=	NP_001289889.1:p.Asp172=
NM_003977.3:c.514G=	NP_003968.3:p.Asp172=
XM_024448761.1:c.514G=	XP_024304529.1:p.Asp172=
NM_003977.4:c.514G= MANE Select	NP_003968.3:p.Asp172=
NM_001302960.2:c.514G=	NP_001289889.1:p.Asp172=
NM_001302959.2:c.337G=	NP_001289888.1:p.Asp113=