Canonical Allele Identifier: CA1980172097

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489648C= , CM000673.2:g.67489648C=	GRCh38
NC_000011.9:g.67257119C= , CM000673.1:g.67257119C=	GRCh37
NC_000011.8:g.67013695C=	NCBI36
NG_008969.1:g.11615C= , LRG_460:g.11615C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.445+193C=
ENST00000528641.7:c.280-390C=	ENSP00000434982.3:n.280-390C=
ENST00000529797.2:n.591C=
ENST00000682324.1:c.468+193C=	ENSP00000508017.1:n.468+193C=
ENST00000682659.1:c.100-390C=	ENSP00000507351.1:n.100-390C=
ENST00000682699.1:c.468+193C=	ENSP00000507935.1:n.468+193C=
ENST00000683237.1:c.468+193C=	ENSP00000507343.1:n.468+193C=
ENST00000683856.1:c.291+193C=	ENSP00000507979.1:n.291+193C=
ENST00000684006.1:c.468+193C=	ENSP00000507269.1:n.468+193C=
ENST00000684657.1:c.288+193C=	ENSP00000507961.1:n.288+193C=
ENST00000279146.8:c.468+193C= MANE Select	ENSP00000279146.3:n.468+193C=
ENST00000279146.7:c.468+193C=	ENSP00000279146.3:n.468+193C=
ENST00000525341.1:c.120+193C=	ENSP00000476993.1:n.120+193C=
ENST00000528641.6:c.280-390C=	ENSP00000434982.2:n.280-390C=
ENST00000529797.1:n.771C=
NM_001302959.1:c.291+193C=	NP_001289888.1:n.291+193C=
NM_001302960.1:c.468+193C=	NP_001289889.1:n.468+193C=
NM_003977.3:c.468+193C=	NP_003968.3:n.468+193C=
XM_024448761.1:c.468+193C=	XP_024304529.1:n.468+193C=
NM_003977.4:c.468+193C= MANE Select	NP_003968.3:n.468+193C=
NM_001302960.2:c.468+193C=	NP_001289889.1:n.468+193C=
NM_001302959.2:c.291+193C=	NP_001289888.1:n.291+193C=