Canonical Allele Identifier: CA1980172045

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489546C= , CM000673.2:g.67489546C=	GRCh38
NC_000011.9:g.67257017C= , CM000673.1:g.67257017C=	GRCh37
NC_000011.8:g.67013593C=	NCBI36
NG_008969.1:g.11513C= , LRG_460:g.11513C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.445+91C=
ENST00000528641.7:c.280-492C=	ENSP00000434982.3:n.280-492C=
ENST00000529797.2:n.489C=
ENST00000682324.1:c.468+91C=	ENSP00000508017.1:n.468+91C=
ENST00000682659.1:c.100-492C=	ENSP00000507351.1:n.100-492C=
ENST00000682699.1:c.468+91C=	ENSP00000507935.1:n.468+91C=
ENST00000683237.1:c.468+91C=	ENSP00000507343.1:n.468+91C=
ENST00000683856.1:c.291+91C=	ENSP00000507979.1:n.291+91C=
ENST00000684006.1:c.468+91C=	ENSP00000507269.1:n.468+91C=
ENST00000684657.1:c.288+91C=	ENSP00000507961.1:n.288+91C=
ENST00000279146.8:c.468+91C= MANE Select	ENSP00000279146.3:n.468+91C=
ENST00000279146.7:c.468+91C=	ENSP00000279146.3:n.468+91C=
ENST00000525341.1:c.120+91C=	ENSP00000476993.1:n.120+91C=
ENST00000528641.6:c.280-492C=	ENSP00000434982.2:n.280-492C=
ENST00000529797.1:n.669C=
NM_001302959.1:c.291+91C=	NP_001289888.1:n.291+91C=
NM_001302960.1:c.468+91C=	NP_001289889.1:n.468+91C=
NM_003977.3:c.468+91C=	NP_003968.3:n.468+91C=
XM_024448761.1:c.468+91C=	XP_024304529.1:n.468+91C=
NM_003977.4:c.468+91C= MANE Select	NP_003968.3:n.468+91C=
NM_001302960.2:c.468+91C=	NP_001289889.1:n.468+91C=
NM_001302959.2:c.291+91C=	NP_001289888.1:n.291+91C=