Canonical Allele Identifier: CA1980172352

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490221C= , CM000673.2:g.67490221C=	GRCh38
NC_000011.9:g.67257692C= , CM000673.1:g.67257692C=	GRCh37
NC_000011.8:g.67014268C=	NCBI36
NG_008969.1:g.12188C= , LRG_460:g.12188C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.622+7C=
ENST00000528641.7:c.456+7C=	ENSP00000434982.3:n.456+7C=
ENST00000529797.2:n.1157+7C=
ENST00000682324.1:c.468+766C=	ENSP00000508017.1:n.468+766C=
ENST00000682659.1:c.276+7C=	ENSP00000507351.1:n.276+7C=
ENST00000682699.1:c.645+7C=	ENSP00000507935.1:n.645+7C=
ENST00000683237.1:c.645+7C=	ENSP00000507343.1:n.645+7C=
ENST00000683856.1:c.468+7C=	ENSP00000507979.1:n.468+7C=
ENST00000684006.1:c.645+7C=	ENSP00000507269.1:n.645+7C=
ENST00000684657.1:c.465+7C=	ENSP00000507961.1:n.465+7C=
ENST00000279146.8:c.645+7C= MANE Select	ENSP00000279146.3:n.645+7C=
ENST00000279146.7:c.645+7C=	ENSP00000279146.3:n.645+7C=
ENST00000525341.1:c.297+7C=	ENSP00000476993.1:n.297+7C=
ENST00000528641.6:c.456+7C=	ENSP00000434982.2:n.456+7C=
NM_001302959.1:c.468+7C=	NP_001289888.1:n.468+7C=
NM_001302960.1:c.645+7C=	NP_001289889.1:n.645+7C=
NM_003977.3:c.645+7C=	NP_003968.3:n.645+7C=
XM_024448761.1:c.645+7C=	XP_024304529.1:n.645+7C=
NM_003977.4:c.645+7C= MANE Select	NP_003968.3:n.645+7C=
NM_001302960.2:c.645+7C=	NP_001289889.1:n.645+7C=
NM_001302959.2:c.468+7C=	NP_001289888.1:n.468+7C=