Canonical Allele Identifier: CA1980170923

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67487061A= , CM000673.2:g.67487061A=	GRCh38
NC_000011.9:g.67254532A= , CM000673.1:g.67254532A=	GRCh37
NC_000011.8:g.67011108A=	NCBI36
NG_008969.1:g.9028A= , LRG_460:g.9028A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.132A=
ENST00000528641.7:c.155A=	ENSP00000434982.3:p.Asp52=
ENST00000529797.2:n.85A=
ENST00000682324.1:c.155A=	ENSP00000508017.1:p.Asp52=
ENST00000682659.1:c.100-2977A=	ENSP00000507351.1:n.100-2977A=
ENST00000682699.1:c.155A=	ENSP00000507935.1:p.Asp52=
ENST00000683237.1:c.155A=	ENSP00000507343.1:p.Asp52=
ENST00000683856.1:c.-23A=	ENSP00000507979.1:n.-23A=
ENST00000684006.1:c.155A=	ENSP00000507269.1:p.Asp52=
ENST00000684657.1:c.100-2206A=	ENSP00000507961.1:n.100-2206A=
ENST00000279146.8:c.155A= MANE Select	ENSP00000279146.3:p.Asp52=
ENST00000279146.7:c.155A=	ENSP00000279146.3:p.Asp52=
ENST00000528641.6:c.155A=	ENSP00000434982.2:p.Asp52=
ENST00000529797.1:n.265A=
NM_001302959.1:c.-23A=	NP_001289888.1:n.-23A=
NM_001302960.1:c.155A=	NP_001289889.1:p.Asp52=
NM_003977.3:c.155A=	NP_003968.3:p.Asp52=
XM_024448761.1:c.155A=	XP_024304529.1:p.Asp52=
NM_003977.4:c.155A= MANE Select	NP_003968.3:p.Asp52=
NM_001302960.2:c.155A=	NP_001289889.1:p.Asp52=
NM_001302959.2:c.-23A=	NP_001289888.1:n.-23A=