Canonical Allele Identifier: CA1980172313

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490136G= , CM000673.2:g.67490136G=	GRCh38
NC_000011.9:g.67257607G= , CM000673.1:g.67257607G=	GRCh37
NC_000011.8:g.67014183G=	NCBI36
NG_008969.1:g.12103G= , LRG_460:g.12103G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.544G=
ENST00000528641.7:c.378G=	ENSP00000434982.3:p.Leu126=
ENST00000529797.2:n.1079G=
ENST00000682324.1:c.468+681G=	ENSP00000508017.1:n.468+681G=
ENST00000682659.1:c.198G=	ENSP00000507351.1:p.Leu66=
ENST00000682699.1:c.567G=	ENSP00000507935.1:p.Leu189=
ENST00000683237.1:c.567G=	ENSP00000507343.1:p.Leu189=
ENST00000683856.1:c.390G=	ENSP00000507979.1:p.Leu130=
ENST00000684006.1:c.567G=	ENSP00000507269.1:p.Leu189=
ENST00000684657.1:c.387G=	ENSP00000507961.1:p.Leu129=
ENST00000279146.8:c.567G= MANE Select	ENSP00000279146.3:p.Leu189=
ENST00000279146.7:c.567G=	ENSP00000279146.3:p.Leu189=
ENST00000525341.1:c.219G=	ENSP00000476993.1:p.Leu73=
ENST00000528641.6:c.378G=	ENSP00000434982.2:p.Leu126=
NM_001302959.1:c.390G=	NP_001289888.1:p.Leu130=
NM_001302960.1:c.567G=	NP_001289889.1:p.Leu189=
NM_003977.3:c.567G=	NP_003968.3:p.Leu189=
XM_024448761.1:c.567G=	XP_024304529.1:p.Leu189=
NM_003977.4:c.567G= MANE Select	NP_003968.3:p.Leu189=
NM_001302960.2:c.567G=	NP_001289889.1:p.Leu189=
NM_001302959.2:c.390G=	NP_001289888.1:p.Leu130=