Canonical Allele Identifier: CA1980172302

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490113A= , CM000673.2:g.67490113A=	GRCh38
NC_000011.9:g.67257584A= , CM000673.1:g.67257584A=	GRCh37
NC_000011.8:g.67014160A=	NCBI36
NG_008969.1:g.12080A= , LRG_460:g.12080A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.521A=
ENST00000528641.7:c.355A=	ENSP00000434982.3:p.Ile119=
ENST00000529797.2:n.1056A=
ENST00000682324.1:c.468+658A=	ENSP00000508017.1:n.468+658A=
ENST00000682659.1:c.175A=	ENSP00000507351.1:p.Ile59=
ENST00000682699.1:c.544A=	ENSP00000507935.1:p.Ile182=
ENST00000683237.1:c.544A=	ENSP00000507343.1:p.Ile182=
ENST00000683856.1:c.367A=	ENSP00000507979.1:p.Ile123=
ENST00000684006.1:c.544A=	ENSP00000507269.1:p.Ile182=
ENST00000684657.1:c.364A=	ENSP00000507961.1:p.Ile122=
ENST00000279146.8:c.544A= MANE Select	ENSP00000279146.3:p.Ile182=
ENST00000279146.7:c.544A=	ENSP00000279146.3:p.Ile182=
ENST00000525341.1:c.196A=	ENSP00000476993.1:p.Ile66=
ENST00000528641.6:c.355A=	ENSP00000434982.2:p.Ile119=
NM_001302959.1:c.367A=	NP_001289888.1:p.Ile123=
NM_001302960.1:c.544A=	NP_001289889.1:p.Ile182=
NM_003977.3:c.544A=	NP_003968.3:p.Ile182=
XM_024448761.1:c.544A=	XP_024304529.1:p.Ile182=
NM_003977.4:c.544A= MANE Select	NP_003968.3:p.Ile182=
NM_001302960.2:c.544A=	NP_001289889.1:p.Ile182=
NM_001302959.2:c.367A=	NP_001289888.1:p.Ile123=