Canonical Allele Identifier: CA1980172721

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490965C= , CM000673.2:g.67490965C=	GRCh38
NC_000011.9:g.67258436C= , CM000673.1:g.67258436C=	GRCh37
NC_000011.8:g.67015012C=	NCBI36
NG_008969.1:g.12932C= , LRG_460:g.12932C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.1272C=
ENST00000528641.7:c.776C=	ENSP00000434982.3:p.Ala259=
ENST00000529797.2:n.1807C=
ENST00000682324.1:c.469-32C=	ENSP00000508017.1:n.469-32C=
ENST00000682659.1:c.596C=	ENSP00000507351.1:p.Ala199=
ENST00000683237.1:c.*105C=	ENSP00000507343.1:n.*105C=
ENST00000683856.1:c.788C=	ENSP00000507979.1:p.Ala263=
ENST00000684006.1:c.*105C=	ENSP00000507269.1:n.*105C=
ENST00000684657.1:c.785C=	ENSP00000507961.1:p.Ala262=
ENST00000279146.8:c.965C= MANE Select	ENSP00000279146.3:p.Ala322=
ENST00000279146.7:c.965C=	ENSP00000279146.3:p.Ala322=
NM_001302959.1:c.788C=	NP_001289888.1:p.Ala263=
NM_001302960.1:c.*105C=	NP_001289889.1:n.*105C=
NM_003977.3:c.965C=	NP_003968.3:p.Ala322=
XM_024448761.1:c.965C=	XP_024304529.1:p.Ala322=
NM_003977.4:c.965C= MANE Select	NP_003968.3:p.Ala322=
NM_001302960.2:c.*105C=	NP_001289889.1:n.*105C=
NM_001302959.2:c.788C=	NP_001289888.1:p.Ala263=