Canonical Allele Identifier: CA1980172422

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490363G= , CM000673.2:g.67490363G=	GRCh38
NC_000011.9:g.67257834G= , CM000673.1:g.67257834G=	GRCh37
NC_000011.8:g.67014410G=	NCBI36
NG_008969.1:g.12330G= , LRG_460:g.12330G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.670G=
ENST00000528641.7:c.504G=	ENSP00000434982.3:p.Thr168=
ENST00000529797.2:n.1205G=
ENST00000682324.1:c.469-634G=	ENSP00000508017.1:n.469-634G=
ENST00000682659.1:c.324G=	ENSP00000507351.1:p.Thr108=
ENST00000682699.1:c.693G=	ENSP00000507935.1:p.Thr231=
ENST00000683237.1:c.693G=	ENSP00000507343.1:p.Thr231=
ENST00000683856.1:c.516G=	ENSP00000507979.1:p.Thr172=
ENST00000684006.1:c.693G=	ENSP00000507269.1:p.Thr231=
ENST00000684657.1:c.513G=	ENSP00000507961.1:p.Thr171=
ENST00000279146.8:c.693G= MANE Select	ENSP00000279146.3:p.Thr231=
ENST00000279146.7:c.693G=	ENSP00000279146.3:p.Thr231=
ENST00000525341.1:c.345G=	ENSP00000476993.1:p.Thr115=
ENST00000528641.6:c.504G=	ENSP00000434982.2:p.Thr168=
NM_001302959.1:c.516G=	NP_001289888.1:p.Thr172=
NM_001302960.1:c.693G=	NP_001289889.1:p.Thr231=
NM_003977.3:c.693G=	NP_003968.3:p.Thr231=
XM_024448761.1:c.693G=	XP_024304529.1:p.Thr231=
NM_003977.4:c.693G= MANE Select	NP_003968.3:p.Thr231=
NM_001302960.2:c.693G=	NP_001289889.1:p.Thr231=
NM_001302959.2:c.516G=	NP_001289888.1:p.Thr172=