Canonical Allele Identifier: CA1980170940

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67487088A= , CM000673.2:g.67487088A=	GRCh38
NC_000011.9:g.67254559A= , CM000673.1:g.67254559A=	GRCh37
NC_000011.8:g.67011135A=	NCBI36
NG_008969.1:g.9055A= , LRG_460:g.9055A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.159A=
ENST00000528641.7:c.182A=	ENSP00000434982.3:p.Glu61=
ENST00000529797.2:n.112A=
ENST00000682324.1:c.182A=	ENSP00000508017.1:p.Glu61=
ENST00000682659.1:c.100-2950A=	ENSP00000507351.1:n.100-2950A=
ENST00000682699.1:c.182A=	ENSP00000507935.1:p.Glu61=
ENST00000683237.1:c.182A=	ENSP00000507343.1:p.Glu61=
ENST00000683856.1:c.5A=	ENSP00000507979.1:p.Glu2=
ENST00000684006.1:c.182A=	ENSP00000507269.1:p.Glu61=
ENST00000684657.1:c.100-2179A=	ENSP00000507961.1:n.100-2179A=
ENST00000279146.8:c.182A= MANE Select	ENSP00000279146.3:p.Glu61=
ENST00000279146.7:c.182A=	ENSP00000279146.3:p.Glu61=
ENST00000528641.6:c.182A=	ENSP00000434982.2:p.Glu61=
ENST00000529797.1:n.292A=
NM_001302959.1:c.5A=	NP_001289888.1:p.Glu2=
NM_001302960.1:c.182A=	NP_001289889.1:p.Glu61=
NM_003977.3:c.182A=	NP_003968.3:p.Glu61=
XM_024448761.1:c.182A=	XP_024304529.1:p.Glu61=
NM_003977.4:c.182A= MANE Select	NP_003968.3:p.Glu61=
NM_001302960.2:c.182A=	NP_001289889.1:p.Glu61=
NM_001302959.2:c.5A=	NP_001289888.1:p.Glu2=