Canonical Allele Identifier: CA1980172287

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490085C= , CM000673.2:g.67490085C=	GRCh38
NC_000011.9:g.67257556C= , CM000673.1:g.67257556C=	GRCh37
NC_000011.8:g.67014132C=	NCBI36
NG_008969.1:g.12052C= , LRG_460:g.12052C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.493C=
ENST00000528641.7:c.327C=	ENSP00000434982.3:p.Asp109=
ENST00000529797.2:n.1028C=
ENST00000682324.1:c.468+630C=	ENSP00000508017.1:n.468+630C=
ENST00000682659.1:c.147C=	ENSP00000507351.1:p.Asp49=
ENST00000682699.1:c.516C=	ENSP00000507935.1:p.Asp172=
ENST00000683237.1:c.516C=	ENSP00000507343.1:p.Asp172=
ENST00000683856.1:c.339C=	ENSP00000507979.1:p.Asp113=
ENST00000684006.1:c.516C=	ENSP00000507269.1:p.Asp172=
ENST00000684657.1:c.336C=	ENSP00000507961.1:p.Asp112=
ENST00000279146.8:c.516C= MANE Select	ENSP00000279146.3:p.Asp172=
ENST00000279146.7:c.516C=	ENSP00000279146.3:p.Asp172=
ENST00000525341.1:c.168C=	ENSP00000476993.1:p.Asp56=
ENST00000528641.6:c.327C=	ENSP00000434982.2:p.Asp109=
NM_001302959.1:c.339C=	NP_001289888.1:p.Asp113=
NM_001302960.1:c.516C=	NP_001289889.1:p.Asp172=
NM_003977.3:c.516C=	NP_003968.3:p.Asp172=
XM_024448761.1:c.516C=	XP_024304529.1:p.Asp172=
NM_003977.4:c.516C= MANE Select	NP_003968.3:p.Asp172=
NM_001302960.2:c.516C=	NP_001289889.1:p.Asp172=
NM_001302959.2:c.339C=	NP_001289888.1:p.Asp113=