Canonical Allele Identifier: CA1980172683

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490889G= , CM000673.2:g.67490889G=	GRCh38
NC_000011.9:g.67258360G= , CM000673.1:g.67258360G=	GRCh37
NC_000011.8:g.67014936G=	NCBI36
NG_008969.1:g.12856G= , LRG_460:g.12856G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.1196G=
ENST00000528641.7:c.700G=	ENSP00000434982.3:p.Ala234=
ENST00000529797.2:n.1731G=
ENST00000682324.1:c.469-108G=	ENSP00000508017.1:n.469-108G=
ENST00000682659.1:c.520G=	ENSP00000507351.1:p.Ala174=
ENST00000682699.1:c.889G=	ENSP00000507935.1:p.Ala297=
ENST00000683237.1:c.*29G=	ENSP00000507343.1:n.*29G=
ENST00000683856.1:c.712G=	ENSP00000507979.1:p.Ala238=
ENST00000684006.1:c.*29G=	ENSP00000507269.1:n.*29G=
ENST00000684657.1:c.709G=	ENSP00000507961.1:p.Ala237=
ENST00000279146.8:c.889G= MANE Select	ENSP00000279146.3:p.Ala297=
ENST00000279146.7:c.889G=	ENSP00000279146.3:p.Ala297=
NM_001302959.1:c.712G=	NP_001289888.1:p.Ala238=
NM_001302960.1:c.*29G=	NP_001289889.1:n.*29G=
NM_003977.3:c.889G=	NP_003968.3:p.Ala297=
XM_024448761.1:c.889G=	XP_024304529.1:p.Ala297=
NM_003977.4:c.889G= MANE Select	NP_003968.3:p.Ala297=
NM_001302960.2:c.*29G=	NP_001289889.1:n.*29G=
NM_001302959.2:c.712G=	NP_001289888.1:p.Ala238=