Canonical Allele Identifier: CA1980172655

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490829G= , CM000673.2:g.67490829G=	GRCh38
NC_000011.9:g.67258300G= , CM000673.1:g.67258300G=	GRCh37
NC_000011.8:g.67014876G=	NCBI36
NG_008969.1:g.12796G= , LRG_460:g.12796G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1136G=
ENST00000528641.7:c.640G=	ENSP00000434982.3:p.Ala214=
ENST00000529797.2:n.1671G=
ENST00000682324.1:c.469-168G=	ENSP00000508017.1:n.469-168G=
ENST00000682659.1:c.460G=	ENSP00000507351.1:p.Ala154=
ENST00000682699.1:c.829G=	ENSP00000507935.1:p.Ala277=
ENST00000683237.1:c.821G=	ENSP00000507343.1:p.Gly274=
ENST00000683856.1:c.652G=	ENSP00000507979.1:p.Ala218=
ENST00000684006.1:c.818G=	ENSP00000507269.1:p.Gly273=
ENST00000684657.1:c.649G=	ENSP00000507961.1:p.Ala217=
ENST00000279146.8:c.829G= MANE Select	ENSP00000279146.3:p.Ala277=
ENST00000279146.7:c.829G=	ENSP00000279146.3:p.Ala277=
ENST00000528641.6:c.640G=	ENSP00000434982.2:p.Ala214=
NM_001302959.1:c.652G=	NP_001289888.1:p.Ala218=
NM_001302960.1:c.821G=	NP_001289889.1:p.Gly274=
NM_003977.3:c.829G=	NP_003968.3:p.Ala277=
XM_024448761.1:c.829G=	XP_024304529.1:p.Ala277=
NM_003977.4:c.829G= MANE Select	NP_003968.3:p.Ala277=
NM_001302960.2:c.821G=	NP_001289889.1:p.Gly274=
NM_001302959.2:c.652G=	NP_001289888.1:p.Ala218=