Canonical Allele Identifier: CA1980172301

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490112T= , CM000673.2:g.67490112T=	GRCh38
NC_000011.9:g.67257583T= , CM000673.1:g.67257583T=	GRCh37
NC_000011.8:g.67014159T=	NCBI36
NG_008969.1:g.12079T= , LRG_460:g.12079T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.520T=
ENST00000528641.7:c.354T=	ENSP00000434982.3:p.Leu118=
ENST00000529797.2:n.1055T=
ENST00000682324.1:c.468+657T=	ENSP00000508017.1:n.468+657T=
ENST00000682659.1:c.174T=	ENSP00000507351.1:p.Leu58=
ENST00000682699.1:c.543T=	ENSP00000507935.1:p.Leu181=
ENST00000683237.1:c.543T=	ENSP00000507343.1:p.Leu181=
ENST00000683856.1:c.366T=	ENSP00000507979.1:p.Leu122=
ENST00000684006.1:c.543T=	ENSP00000507269.1:p.Leu181=
ENST00000684657.1:c.363T=	ENSP00000507961.1:p.Leu121=
ENST00000279146.8:c.543T= MANE Select	ENSP00000279146.3:p.Leu181=
ENST00000279146.7:c.543T=	ENSP00000279146.3:p.Leu181=
ENST00000525341.1:c.195T=	ENSP00000476993.1:p.Leu65=
ENST00000528641.6:c.354T=	ENSP00000434982.2:p.Leu118=
NM_001302959.1:c.366T=	NP_001289888.1:p.Leu122=
NM_001302960.1:c.543T=	NP_001289889.1:p.Leu181=
NM_003977.3:c.543T=	NP_003968.3:p.Leu181=
XM_024448761.1:c.543T=	XP_024304529.1:p.Leu181=
NM_003977.4:c.543T= MANE Select	NP_003968.3:p.Leu181=
NM_001302960.2:c.543T=	NP_001289889.1:p.Leu181=
NM_001302959.2:c.366T=	NP_001289888.1:p.Leu122=