Canonical Allele Identifier: CA1980172467

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490445A= , CM000673.2:g.67490445A=	GRCh38
NC_000011.9:g.67257916A= , CM000673.1:g.67257916A=	GRCh37
NC_000011.8:g.67014492A=	NCBI36
NG_008969.1:g.12412A= , LRG_460:g.12412A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.752A=
ENST00000528641.7:c.586A=	ENSP00000434982.3:p.Asn196=
ENST00000529797.2:n.1287A=
ENST00000682324.1:c.469-552A=	ENSP00000508017.1:n.469-552A=
ENST00000682659.1:c.406A=	ENSP00000507351.1:p.Asn136=
ENST00000682699.1:c.775A=	ENSP00000507935.1:p.Asn259=
ENST00000683237.1:c.775A=	ENSP00000507343.1:p.Asn259=
ENST00000683856.1:c.598A=	ENSP00000507979.1:p.Asn200=
ENST00000684006.1:c.775A=	ENSP00000507269.1:p.Asn259=
ENST00000684657.1:c.595A=	ENSP00000507961.1:p.Asn199=
ENST00000279146.8:c.775A= MANE Select	ENSP00000279146.3:p.Asn259=
ENST00000279146.7:c.775A=	ENSP00000279146.3:p.Asn259=
ENST00000525341.1:c.427A=	ENSP00000476993.1:p.Asn143=
ENST00000528641.6:c.586A=	ENSP00000434982.2:p.Asn196=
NM_001302959.1:c.598A=	NP_001289888.1:p.Asn200=
NM_001302960.1:c.775A=	NP_001289889.1:p.Asn259=
NM_003977.3:c.775A=	NP_003968.3:p.Asn259=
XM_024448761.1:c.775A=	XP_024304529.1:p.Asn259=
NM_003977.4:c.775A= MANE Select	NP_003968.3:p.Asn259=
NM_001302960.2:c.775A=	NP_001289889.1:p.Asn259=
NM_001302959.2:c.598A=	NP_001289888.1:p.Asn200=