Canonical Allele Identifier: CA1980172563

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490627G= , CM000673.2:g.67490627G=	GRCh38
NC_000011.9:g.67258098G= , CM000673.1:g.67258098G=	GRCh37
NC_000011.8:g.67014674G=	NCBI36
NG_008969.1:g.12594G= , LRG_460:g.12594G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.934G=
ENST00000528641.7:c.599-161G=	ENSP00000434982.3:n.599-161G=
ENST00000529797.2:n.1469G=
ENST00000682324.1:c.469-370G=	ENSP00000508017.1:n.469-370G=
ENST00000682659.1:c.419-161G=	ENSP00000507351.1:n.419-161G=
ENST00000682699.1:c.788-161G=	ENSP00000507935.1:n.788-161G=
ENST00000683237.1:c.780-161G=	ENSP00000507343.1:n.780-161G=
ENST00000683856.1:c.611-161G=	ENSP00000507979.1:n.611-161G=
ENST00000684006.1:c.787+170G=	ENSP00000507269.1:n.787+170G=
ENST00000684657.1:c.608-161G=	ENSP00000507961.1:n.608-161G=
ENST00000279146.8:c.788-161G= MANE Select	ENSP00000279146.3:n.788-161G=
ENST00000279146.7:c.788-161G=	ENSP00000279146.3:n.788-161G=
ENST00000525341.1:c.609G=	ENSP00000476993.1:n.609G=
ENST00000528641.6:c.599-161G=	ENSP00000434982.2:n.599-161G=
NM_001302959.1:c.611-161G=	NP_001289888.1:n.611-161G=
NM_001302960.1:c.780-161G=	NP_001289889.1:n.780-161G=
NM_003977.3:c.788-161G=	NP_003968.3:n.788-161G=
XM_024448761.1:c.788-161G=	XP_024304529.1:n.788-161G=
NM_003977.4:c.788-161G= MANE Select	NP_003968.3:n.788-161G=
NM_001302960.2:c.780-161G=	NP_001289889.1:n.780-161G=
NM_001302959.2:c.611-161G=	NP_001289888.1:n.611-161G=