Canonical Allele Identifier: CA1980172411

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490332_67490333delinsCT , CM000673.2:g.67490332_67490333delinsCT	GRCh38
NC_000011.9:g.67257803_67257804delinsCT , CM000673.1:g.67257803_67257804delinsCT	GRCh37
NC_000011.8:g.67014379_67014380delinsCT	NCBI36
NG_008969.1:g.12299_12300delinsCT , LRG_460:g.12299_12300delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.639_640delinsCT
ENST00000528641.7:c.473_474delinsCT	ENSP00000434982.3:p.Pro158=
ENST00000529797.2:n.1174_1175delinsCT
ENST00000682324.1:c.469-665_469-664delinsCT	ENSP00000508017.1:n.469-665_469-664delins...
ENST00000682659.1:c.293_294delinsCT	ENSP00000507351.1:p.Pro98=
ENST00000682699.1:c.662_663delinsCT	ENSP00000507935.1:p.Pro221=
ENST00000683237.1:c.662_663delinsCT	ENSP00000507343.1:p.Pro221=
ENST00000683856.1:c.485_486delinsCT	ENSP00000507979.1:p.Pro162=
ENST00000684006.1:c.662_663delinsCT	ENSP00000507269.1:p.Pro221=
ENST00000684657.1:c.482_483delinsCT	ENSP00000507961.1:p.Pro161=
ENST00000279146.8:c.662_663delinsCT MANE Select	ENSP00000279146.3:p.Pro221=
ENST00000279146.7:c.662_663delinsCT	ENSP00000279146.3:p.Pro221=
ENST00000525341.1:c.314_315delinsCT	ENSP00000476993.1:p.Pro105=
ENST00000528641.6:c.473_474delinsCT	ENSP00000434982.2:p.Pro158=
NM_001302959.1:c.485_486delinsCT	NP_001289888.1:p.Pro162=
NM_001302960.1:c.662_663delinsCT	NP_001289889.1:p.Pro221=
NM_003977.3:c.662_663delinsCT	NP_003968.3:p.Pro221=
XM_024448761.1:c.662_663delinsCT	XP_024304529.1:p.Pro221=
NM_003977.4:c.662_663delinsCT MANE Select	NP_003968.3:p.Pro221=
NM_001302960.2:c.662_663delinsCT	NP_001289889.1:p.Pro221=
NM_001302959.2:c.485_486delinsCT	NP_001289888.1:p.Pro162=