Canonical Allele Identifier: CA1980172672

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490866C= , CM000673.2:g.67490866C=	GRCh38
NC_000011.9:g.67258337C= , CM000673.1:g.67258337C=	GRCh37
NC_000011.8:g.67014913C=	NCBI36
NG_008969.1:g.12833C= , LRG_460:g.12833C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1173C=
ENST00000528641.7:c.677C=	ENSP00000434982.3:p.Ala226=
ENST00000529797.2:n.1708C=
ENST00000682324.1:c.469-131C=	ENSP00000508017.1:n.469-131C=
ENST00000682659.1:c.497C=	ENSP00000507351.1:p.Ala166=
ENST00000682699.1:c.866C=	ENSP00000507935.1:p.Ala289=
ENST00000683237.1:c.*6C=	ENSP00000507343.1:n.*6C=
ENST00000683856.1:c.689C=	ENSP00000507979.1:p.Ala230=
ENST00000684006.1:c.*6C=	ENSP00000507269.1:n.*6C=
ENST00000684657.1:c.686C=	ENSP00000507961.1:p.Ala229=
ENST00000279146.8:c.866C= MANE Select	ENSP00000279146.3:p.Ala289=
ENST00000279146.7:c.866C=	ENSP00000279146.3:p.Ala289=
ENST00000528641.6:c.677C=	ENSP00000434982.2:p.Ala226=
NM_001302959.1:c.689C=	NP_001289888.1:p.Ala230=
NM_001302960.1:c.*6C=	NP_001289889.1:n.*6C=
NM_003977.3:c.866C=	NP_003968.3:p.Ala289=
XM_024448761.1:c.866C=	XP_024304529.1:p.Ala289=
NM_003977.4:c.866C= MANE Select	NP_003968.3:p.Ala289=
NM_001302960.2:c.*6C=	NP_001289889.1:n.*6C=
NM_001302959.2:c.689C=	NP_001289888.1:p.Ala230=