Canonical Allele Identifier: CA1980172006

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489468C= , CM000673.2:g.67489468C=	GRCh38
NC_000011.9:g.67256939C= , CM000673.1:g.67256939C=	GRCh37
NC_000011.8:g.67013515C=	NCBI36
NG_008969.1:g.11435C= , LRG_460:g.11435C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.445+13C=
ENST00000528641.7:c.280-570C=	ENSP00000434982.3:n.280-570C=
ENST00000529797.2:n.411C=
ENST00000682324.1:c.468+13C=	ENSP00000508017.1:n.468+13C=
ENST00000682659.1:c.100-570C=	ENSP00000507351.1:n.100-570C=
ENST00000682699.1:c.468+13C=	ENSP00000507935.1:n.468+13C=
ENST00000683237.1:c.468+13C=	ENSP00000507343.1:n.468+13C=
ENST00000683856.1:c.291+13C=	ENSP00000507979.1:n.291+13C=
ENST00000684006.1:c.468+13C=	ENSP00000507269.1:n.468+13C=
ENST00000684657.1:c.288+13C=	ENSP00000507961.1:n.288+13C=
ENST00000279146.8:c.468+13C= MANE Select	ENSP00000279146.3:n.468+13C=
ENST00000279146.7:c.468+13C=	ENSP00000279146.3:n.468+13C=
ENST00000525341.1:c.120+13C=	ENSP00000476993.1:n.120+13C=
ENST00000528641.6:c.280-570C=	ENSP00000434982.2:n.280-570C=
ENST00000529797.1:n.591C=
NM_001302959.1:c.291+13C=	NP_001289888.1:n.291+13C=
NM_001302960.1:c.468+13C=	NP_001289889.1:n.468+13C=
NM_003977.3:c.468+13C=	NP_003968.3:n.468+13C=
XM_024448761.1:c.468+13C=	XP_024304529.1:n.468+13C=
NM_003977.4:c.468+13C= MANE Select	NP_003968.3:n.468+13C=
NM_001302960.2:c.468+13C=	NP_001289889.1:n.468+13C=
NM_001302959.2:c.291+13C=	NP_001289888.1:n.291+13C=