Canonical Allele Identifier: CA1980172682

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490886C= , CM000673.2:g.67490886C=	GRCh38
NC_000011.9:g.67258357C= , CM000673.1:g.67258357C=	GRCh37
NC_000011.8:g.67014933C=	NCBI36
NG_008969.1:g.12853C= , LRG_460:g.12853C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1193C=
ENST00000528641.7:c.697C=	ENSP00000434982.3:p.Pro233=
ENST00000529797.2:n.1728C=
ENST00000682324.1:c.469-111C=	ENSP00000508017.1:n.469-111C=
ENST00000682659.1:c.517C=	ENSP00000507351.1:p.Pro173=
ENST00000682699.1:c.886C=	ENSP00000507935.1:p.Pro296=
ENST00000683237.1:c.*26C=	ENSP00000507343.1:n.*26C=
ENST00000683856.1:c.709C=	ENSP00000507979.1:p.Pro237=
ENST00000684006.1:c.*26C=	ENSP00000507269.1:n.*26C=
ENST00000684657.1:c.706C=	ENSP00000507961.1:p.Pro236=
ENST00000279146.8:c.886C= MANE Select	ENSP00000279146.3:p.Pro296=
ENST00000279146.7:c.886C=	ENSP00000279146.3:p.Pro296=
ENST00000528641.6:c.697C=
NM_001302959.1:c.709C=	NP_001289888.1:p.Pro237=
NM_001302960.1:c.*26C=	NP_001289889.1:n.*26C=
NM_003977.3:c.886C=	NP_003968.3:p.Pro296=
XM_024448761.1:c.886C=	XP_024304529.1:p.Pro296=
NM_003977.4:c.886C= MANE Select	NP_003968.3:p.Pro296=
NM_001302960.2:c.*26C=	NP_001289889.1:n.*26C=
NM_001302959.2:c.709C=	NP_001289888.1:p.Pro237=