Canonical Allele Identifier: CA1980172680

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490884A= , CM000673.2:g.67490884A=	GRCh38
NC_000011.9:g.67258355A= , CM000673.1:g.67258355A=	GRCh37
NC_000011.8:g.67014931A=	NCBI36
NG_008969.1:g.12851A= , LRG_460:g.12851A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1191A=
ENST00000528641.7:c.695A=	ENSP00000434982.3:p.Asp232=
ENST00000529797.2:n.1726A=
ENST00000682324.1:c.469-113A=	ENSP00000508017.1:n.469-113A=
ENST00000682659.1:c.515A=	ENSP00000507351.1:p.Asp172=
ENST00000682699.1:c.884A=	ENSP00000507935.1:p.Asp295=
ENST00000683237.1:c.*24A=	ENSP00000507343.1:n.*24A=
ENST00000683856.1:c.707A=	ENSP00000507979.1:p.Asp236=
ENST00000684006.1:c.*24A=	ENSP00000507269.1:n.*24A=
ENST00000684657.1:c.704A=	ENSP00000507961.1:p.Asp235=
ENST00000279146.8:c.884A= MANE Select	ENSP00000279146.3:p.Asp295=
ENST00000279146.7:c.884A=	ENSP00000279146.3:p.Asp295=
ENST00000528641.6:c.695A=	ENSP00000434982.2:p.Asp232=
NM_001302959.1:c.707A=	NP_001289888.1:p.Asp236=
NM_001302960.1:c.*24A=	NP_001289889.1:n.*24A=
NM_003977.3:c.884A=	NP_003968.3:p.Asp295=
XM_024448761.1:c.884A=	XP_024304529.1:p.Asp295=
NM_003977.4:c.884A= MANE Select	NP_003968.3:p.Asp295=
NM_001302960.2:c.*24A=	NP_001289889.1:n.*24A=
NM_001302959.2:c.707A=	NP_001289888.1:p.Asp236=