Canonical Allele Identifier: CA1980172664

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490852C= , CM000673.2:g.67490852C=	GRCh38
NC_000011.9:g.67258323C= , CM000673.1:g.67258323C=	GRCh37
NC_000011.8:g.67014899C=	NCBI36
NG_008969.1:g.12819C= , LRG_460:g.12819C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1159C=
ENST00000528641.7:c.663C=	ENSP00000434982.3:p.Ala221=
ENST00000529797.2:n.1694C=
ENST00000682324.1:c.469-145C=	ENSP00000508017.1:n.469-145C=
ENST00000682659.1:c.483C=	ENSP00000507351.1:p.Ala161=
ENST00000682699.1:c.852C=	ENSP00000507935.1:p.Ala284=
ENST00000683237.1:c.844C=	ENSP00000507343.1:p.Pro282=
ENST00000683856.1:c.675C=	ENSP00000507979.1:p.Ala225=
ENST00000684006.1:c.841C=	ENSP00000507269.1:p.Pro281=
ENST00000684657.1:c.672C=	ENSP00000507961.1:p.Ala224=
ENST00000279146.8:c.852C= MANE Select	ENSP00000279146.3:p.Ala284=
ENST00000279146.7:c.852C=	ENSP00000279146.3:p.Ala284=
ENST00000528641.6:c.663C=	ENSP00000434982.2:p.Ala221=
NM_001302959.1:c.675C=	NP_001289888.1:p.Ala225=
NM_001302960.1:c.844C=	NP_001289889.1:p.Pro282=
NM_003977.3:c.852C=	NP_003968.3:p.Ala284=
XM_024448761.1:c.852C=	XP_024304529.1:p.Ala284=
NM_003977.4:c.852C= MANE Select	NP_003968.3:p.Ala284=
NM_001302960.2:c.844C=	NP_001289889.1:p.Pro282=
NM_001302959.2:c.675C=	NP_001289888.1:p.Ala225=