Canonical Allele Identifier: CA1980172661

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490836G= , CM000673.2:g.67490836G=	GRCh38
NC_000011.9:g.67258307G= , CM000673.1:g.67258307G=	GRCh37
NC_000011.8:g.67014883G=	NCBI36
NG_008969.1:g.12803G= , LRG_460:g.12803G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.1143G=
ENST00000528641.7:c.647G=	ENSP00000434982.3:p.Trp216=
ENST00000529797.2:n.1678G=
ENST00000682324.1:c.469-161G=	ENSP00000508017.1:n.469-161G=
ENST00000682659.1:c.467G=	ENSP00000507351.1:p.Trp156=
ENST00000682699.1:c.836G=	ENSP00000507935.1:p.Trp279=
ENST00000683237.1:c.828G=	ENSP00000507343.1:p.Val276=
ENST00000683856.1:c.659G=	ENSP00000507979.1:p.Trp220=
ENST00000684006.1:c.825G=	ENSP00000507269.1:p.Val275=
ENST00000684657.1:c.656G=	ENSP00000507961.1:p.Trp219=
ENST00000279146.8:c.836G= MANE Select	ENSP00000279146.3:p.Trp279=
ENST00000279146.7:c.836G=	ENSP00000279146.3:p.Trp279=
ENST00000528641.6:c.647G=	ENSP00000434982.2:p.Trp216=
NM_001302959.1:c.659G=	NP_001289888.1:p.Trp220=
NM_001302960.1:c.828G=	NP_001289889.1:p.Val276=
NM_003977.3:c.836G=	NP_003968.3:p.Trp279=
XM_024448761.1:c.836G=	XP_024304529.1:p.Trp279=
NM_003977.4:c.836G= MANE Select	NP_003968.3:p.Trp279=
NM_001302960.2:c.828G=	NP_001289889.1:p.Val276=
NM_001302959.2:c.659G=	NP_001289888.1:p.Trp220=