Canonical Allele Identifier: CA1980172100

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489651C= , CM000673.2:g.67489651C=	GRCh38
NC_000011.9:g.67257122C= , CM000673.1:g.67257122C=	GRCh37
NC_000011.8:g.67013698C=	NCBI36
NG_008969.1:g.11618C= , LRG_460:g.11618C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.445+196C=
ENST00000528641.7:c.280-387C=	ENSP00000434982.3:n.280-387C=
ENST00000529797.2:n.594C=
ENST00000682324.1:c.468+196C=	ENSP00000508017.1:n.468+196C=
ENST00000682659.1:c.100-387C=	ENSP00000507351.1:n.100-387C=
ENST00000682699.1:c.468+196C=	ENSP00000507935.1:n.468+196C=
ENST00000683237.1:c.468+196C=	ENSP00000507343.1:n.468+196C=
ENST00000683856.1:c.291+196C=	ENSP00000507979.1:n.291+196C=
ENST00000684006.1:c.468+196C=	ENSP00000507269.1:n.468+196C=
ENST00000684657.1:c.288+196C=	ENSP00000507961.1:n.288+196C=
ENST00000279146.8:c.468+196C= MANE Select	ENSP00000279146.3:n.468+196C=
ENST00000279146.7:c.468+196C=	ENSP00000279146.3:n.468+196C=
ENST00000525341.1:c.120+196C=	ENSP00000476993.1:n.120+196C=
ENST00000528641.6:c.280-387C=	ENSP00000434982.2:n.280-387C=
ENST00000529797.1:n.774C=
NM_001302959.1:c.291+196C=	NP_001289888.1:n.291+196C=
NM_001302960.1:c.468+196C=	NP_001289889.1:n.468+196C=
NM_003977.3:c.468+196C=	NP_003968.3:n.468+196C=
XM_024448761.1:c.468+196C=	XP_024304529.1:n.468+196C=
NM_003977.4:c.468+196C= MANE Select	NP_003968.3:n.468+196C=
NM_001302960.2:c.468+196C=	NP_001289889.1:n.468+196C=
NM_001302959.2:c.291+196C=	NP_001289888.1:n.291+196C=