Canonical Allele Identifier: CA1980172415

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490346C= , CM000673.2:g.67490346C=	GRCh38
NC_000011.9:g.67257817C= , CM000673.1:g.67257817C=	GRCh37
NC_000011.8:g.67014393C=	NCBI36
NG_008969.1:g.12313C= , LRG_460:g.12313C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.653C=
ENST00000528641.7:c.487C=	ENSP00000434982.3:p.Leu163=
ENST00000529797.2:n.1188C=
ENST00000682324.1:c.469-651C=	ENSP00000508017.1:n.469-651C=
ENST00000682659.1:c.307C=	ENSP00000507351.1:p.Leu103=
ENST00000682699.1:c.676C=	ENSP00000507935.1:p.Leu226=
ENST00000683237.1:c.676C=	ENSP00000507343.1:p.Leu226=
ENST00000683856.1:c.499C=	ENSP00000507979.1:p.Leu167=
ENST00000684006.1:c.676C=	ENSP00000507269.1:p.Leu226=
ENST00000684657.1:c.496C=	ENSP00000507961.1:p.Leu166=
ENST00000279146.8:c.676C= MANE Select	ENSP00000279146.3:p.Leu226=
ENST00000279146.7:c.676C=	ENSP00000279146.3:p.Leu226=
ENST00000525341.1:c.328C=	ENSP00000476993.1:p.Leu110=
ENST00000528641.6:c.487C=	ENSP00000434982.2:p.Leu163=
NM_001302959.1:c.499C=	NP_001289888.1:p.Leu167=
NM_001302960.1:c.676C=	NP_001289889.1:p.Leu226=
NM_003977.3:c.676C=	NP_003968.3:p.Leu226=
XM_024448761.1:c.676C=	XP_024304529.1:p.Leu226=
NM_003977.4:c.676C= MANE Select	NP_003968.3:p.Leu226=
NM_001302960.2:c.676C=	NP_001289889.1:p.Leu226=
NM_001302959.2:c.499C=	NP_001289888.1:p.Leu167=