Canonical Allele Identifier: CA1980172263

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490036A= , CM000673.2:g.67490036A=	GRCh38
NC_000011.9:g.67257507A= , CM000673.1:g.67257507A=	GRCh37
NC_000011.8:g.67014083A=	NCBI36
NG_008969.1:g.12003A= , LRG_460:g.12003A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.446-2A=
ENST00000528641.7:c.280-2A=	ENSP00000434982.3:n.280-2A=
ENST00000529797.2:n.979A=
ENST00000682324.1:c.468+581A=	ENSP00000508017.1:n.468+581A=
ENST00000682659.1:c.100-2A=	ENSP00000507351.1:n.100-2A=
ENST00000682699.1:c.469-2A=	ENSP00000507935.1:n.469-2A=
ENST00000683237.1:c.469-2A=	ENSP00000507343.1:n.469-2A=
ENST00000683856.1:c.292-2A=	ENSP00000507979.1:n.292-2A=
ENST00000684006.1:c.469-2A=	ENSP00000507269.1:n.469-2A=
ENST00000684657.1:c.289-2A=	ENSP00000507961.1:n.289-2A=
ENST00000279146.8:c.469-2A= MANE Select	ENSP00000279146.3:n.469-2A=
ENST00000279146.7:c.469-2A=	ENSP00000279146.3:n.469-2A=
ENST00000525341.1:c.121-2A=	ENSP00000476993.1:n.121-2A=
ENST00000528641.6:c.280-2A=	ENSP00000434982.2:n.280-2A=
NM_001302959.1:c.292-2A=	NP_001289888.1:n.292-2A=
NM_001302960.1:c.469-2A=	NP_001289889.1:n.469-2A=
NM_003977.3:c.469-2A=	NP_003968.3:n.469-2A=
XM_024448761.1:c.469-2A=	XP_024304529.1:n.469-2A=
NM_003977.4:c.469-2A= MANE Select	NP_003968.3:n.469-2A=
NM_001302960.2:c.469-2A=	NP_001289889.1:n.469-2A=
NM_001302959.2:c.292-2A=	NP_001289888.1:n.292-2A=