Canonical Allele Identifier: CA1980172283

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490075C= , CM000673.2:g.67490075C=	GRCh38
NC_000011.9:g.67257546C= , CM000673.1:g.67257546C=	GRCh37
NC_000011.8:g.67014122C=	NCBI36
NG_008969.1:g.12042C= , LRG_460:g.12042C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.483C=
ENST00000528641.7:c.317C=	ENSP00000434982.3:p.Ala106=
ENST00000529797.2:n.1018C=
ENST00000682324.1:c.468+620C=	ENSP00000508017.1:n.468+620C=
ENST00000682659.1:c.137C=	ENSP00000507351.1:p.Ala46=
ENST00000682699.1:c.506C=	ENSP00000507935.1:p.Ala169=
ENST00000683237.1:c.506C=	ENSP00000507343.1:p.Ala169=
ENST00000683856.1:c.329C=	ENSP00000507979.1:p.Ala110=
ENST00000684006.1:c.506C=	ENSP00000507269.1:p.Ala169=
ENST00000684657.1:c.326C=	ENSP00000507961.1:p.Ala109=
ENST00000279146.8:c.506C= MANE Select	ENSP00000279146.3:p.Ala169=
ENST00000279146.7:c.506C=	ENSP00000279146.3:p.Ala169=
ENST00000525341.1:c.158C=	ENSP00000476993.1:p.Ala53=
ENST00000528641.6:c.317C=	ENSP00000434982.2:p.Ala106=
NM_001302959.1:c.329C=	NP_001289888.1:p.Ala110=
NM_001302960.1:c.506C=	NP_001289889.1:p.Ala169=
NM_003977.3:c.506C=	NP_003968.3:p.Ala169=
XM_024448761.1:c.506C=	XP_024304529.1:p.Ala169=
NM_003977.4:c.506C= MANE Select	NP_003968.3:p.Ala169=
NM_001302960.2:c.506C=	NP_001289889.1:p.Ala169=
NM_001302959.2:c.329C=	NP_001289888.1:p.Ala110=