Canonical Allele Identifier: CA1980172326

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490160G= , CM000673.2:g.67490160G=	GRCh38
NC_000011.9:g.67257631G= , CM000673.1:g.67257631G=	GRCh37
NC_000011.8:g.67014207G=	NCBI36
NG_008969.1:g.12127G= , LRG_460:g.12127G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.568G=
ENST00000528641.7:c.402G=	ENSP00000434982.3:p.Glu134=
ENST00000529797.2:n.1103G=
ENST00000682324.1:c.468+705G=	ENSP00000508017.1:n.468+705G=
ENST00000682659.1:c.222G=	ENSP00000507351.1:p.Glu74=
ENST00000682699.1:c.591G=	ENSP00000507935.1:p.Glu197=
ENST00000683237.1:c.591G=	ENSP00000507343.1:p.Glu197=
ENST00000683856.1:c.414G=	ENSP00000507979.1:p.Glu138=
ENST00000684006.1:c.591G=	ENSP00000507269.1:p.Glu197=
ENST00000684657.1:c.411G=	ENSP00000507961.1:p.Glu137=
ENST00000279146.8:c.591G= MANE Select	ENSP00000279146.3:p.Glu197=
ENST00000279146.7:c.591G=	ENSP00000279146.3:p.Glu197=
ENST00000525341.1:c.243G=	ENSP00000476993.1:p.Glu81=
ENST00000528641.6:c.402G=	ENSP00000434982.2:p.Glu134=
NM_001302959.1:c.414G=	NP_001289888.1:p.Glu138=
NM_001302960.1:c.591G=	NP_001289889.1:p.Glu197=
NM_003977.3:c.591G=	NP_003968.3:p.Glu197=
XM_024448761.1:c.591G=	XP_024304529.1:p.Glu197=
NM_003977.4:c.591G= MANE Select	NP_003968.3:p.Glu197=
NM_001302960.2:c.591G=	NP_001289889.1:p.Glu197=
NM_001302959.2:c.414G=	NP_001289888.1:p.Glu138=