Canonical Allele Identifier: CA1980172278

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490064G= , CM000673.2:g.67490064G=	GRCh38
NC_000011.9:g.67257535G= , CM000673.1:g.67257535G=	GRCh37
NC_000011.8:g.67014111G=	NCBI36
NG_008969.1:g.12031G= , LRG_460:g.12031G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.472G=
ENST00000528641.7:c.306G=	ENSP00000434982.3:p.Gln102=
ENST00000529797.2:n.1007G=
ENST00000682324.1:c.468+609G=	ENSP00000508017.1:n.468+609G=
ENST00000682659.1:c.126G=	ENSP00000507351.1:p.Gln42=
ENST00000682699.1:c.495G=	ENSP00000507935.1:p.Gln165=
ENST00000683237.1:c.495G=	ENSP00000507343.1:p.Gln165=
ENST00000683856.1:c.318G=	ENSP00000507979.1:p.Gln106=
ENST00000684006.1:c.495G=	ENSP00000507269.1:p.Gln165=
ENST00000684657.1:c.315G=	ENSP00000507961.1:p.Gln105=
ENST00000279146.8:c.495G= MANE Select	ENSP00000279146.3:p.Gln165=
ENST00000279146.7:c.495G=	ENSP00000279146.3:p.Gln165=
ENST00000525341.1:c.147G=	ENSP00000476993.1:p.Gln49=
ENST00000528641.6:c.306G=	ENSP00000434982.2:p.Gln102=
NM_001302959.1:c.318G=	NP_001289888.1:p.Gln106=
NM_001302960.1:c.495G=	NP_001289889.1:p.Gln165=
NM_003977.3:c.495G=	NP_003968.3:p.Gln165=
XM_024448761.1:c.495G=	XP_024304529.1:p.Gln165=
NM_003977.4:c.495G= MANE Select	NP_003968.3:p.Gln165=
NM_001302960.2:c.495G=	NP_001289889.1:p.Gln165=
NM_001302959.2:c.318G=	NP_001289888.1:p.Gln106=