Canonical Allele Identifier: CA1980172730

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490979A= , CM000673.2:g.67490979A=	GRCh38
NC_000011.9:g.67258450A= , CM000673.1:g.67258450A=	GRCh37
NC_000011.8:g.67015026A=	NCBI36
NG_008969.1:g.12946A= , LRG_460:g.12946A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1286A=
ENST00000528641.7:c.790A=	ENSP00000434982.3:p.Ile264=
ENST00000529797.2:n.1821A=
ENST00000682324.1:c.469-18A=	ENSP00000508017.1:n.469-18A=
ENST00000682659.1:c.610A=	ENSP00000507351.1:p.Ile204=
ENST00000683237.1:c.*119A=	ENSP00000507343.1:n.*119A=
ENST00000683856.1:c.802A=	ENSP00000507979.1:p.Ile268=
ENST00000684006.1:c.*119A=	ENSP00000507269.1:n.*119A=
ENST00000684657.1:c.799A=	ENSP00000507961.1:p.Ile267=
ENST00000279146.8:c.979A= MANE Select	ENSP00000279146.3:p.Ile327=
ENST00000279146.7:c.979A=	ENSP00000279146.3:p.Ile327=
NM_001302959.1:c.802A=	NP_001289888.1:p.Ile268=
NM_001302960.1:c.*119A=	NP_001289889.1:n.*119A=
NM_003977.3:c.979A=	NP_003968.3:p.Ile327=
XM_024448761.1:c.979A=	XP_024304529.1:p.Ile327=
NM_003977.4:c.979A= MANE Select	NP_003968.3:p.Ile327=
NM_001302960.2:c.*119A=	NP_001289889.1:n.*119A=
NM_001302959.2:c.802A=	NP_001289888.1:p.Ile268=