Canonical Allele Identifier: CA1980172486

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490477C= , CM000673.2:g.67490477C=	GRCh38
NC_000011.9:g.67257948C= , CM000673.1:g.67257948C=	GRCh37
NC_000011.8:g.67014524C=	NCBI36
NG_008969.1:g.12444C= , LRG_460:g.12444C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.784C=
ENST00000528641.7:c.598+20C=	ENSP00000434982.3:n.598+20C=
ENST00000529797.2:n.1319C=
ENST00000682324.1:c.469-520C=	ENSP00000508017.1:n.469-520C=
ENST00000682659.1:c.418+20C=	ENSP00000507351.1:n.418+20C=
ENST00000682699.1:c.787+20C=	ENSP00000507935.1:n.787+20C=
ENST00000683237.1:c.779+28C=	ENSP00000507343.1:n.779+28C=
ENST00000683856.1:c.610+20C=	ENSP00000507979.1:n.610+20C=
ENST00000684006.1:c.787+20C=	ENSP00000507269.1:n.787+20C=
ENST00000684657.1:c.607+20C=	ENSP00000507961.1:n.607+20C=
ENST00000279146.8:c.787+20C= MANE Select	ENSP00000279146.3:n.787+20C=
ENST00000279146.7:c.787+20C=	ENSP00000279146.3:n.787+20C=
ENST00000525341.1:c.459C=	ENSP00000476993.1:p.Gly153=
ENST00000528641.6:c.598+20C=	ENSP00000434982.2:n.598+20C=
NM_001302959.1:c.610+20C=	NP_001289888.1:n.610+20C=
NM_001302960.1:c.779+28C=	NP_001289889.1:n.779+28C=
NM_003977.3:c.787+20C=	NP_003968.3:n.787+20C=
XM_024448761.1:c.787+20C=	XP_024304529.1:n.787+20C=
NM_003977.4:c.787+20C= MANE Select	NP_003968.3:n.787+20C=
NM_001302960.2:c.779+28C=	NP_001289889.1:n.779+28C=
NM_001302959.2:c.610+20C=	NP_001289888.1:n.610+20C=