Canonical Allele Identifier: CA1980172694

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490910C= , CM000673.2:g.67490910C=	GRCh38
NC_000011.9:g.67258381C= , CM000673.1:g.67258381C=	GRCh37
NC_000011.8:g.67014957C=	NCBI36
NG_008969.1:g.12877C= , LRG_460:g.12877C=

Transcript Alleles

HGVS	Amino-acid Change
NM_003977.4:c.910C= MANE Select	NP_003968.3:p.Arg304=
ENST00000279146.8:c.910C= MANE Select	ENSP00000279146.3:p.Arg304=
NM_001302959.1:c.733C=	NP_001289888.1:p.Arg245=
NM_001302959.2:c.733C=	NP_001289888.1:p.Arg245=
NM_001302960.1:c.*50C=	NP_001289889.1:n.*50C=
NM_001302960.2:c.*50C=	NP_001289889.1:n.*50C=
NM_003977.3:c.910C=	NP_003968.3:p.Arg304=
ENST00000279146.7:c.910C=	ENSP00000279146.3:p.Arg304=
ENST00000525341.2:c.1217C=
ENST00000528641.7:c.721C=	ENSP00000434982.3:p.Arg241=
ENST00000529797.2:n.1752C=
ENST00000682324.1:c.469-87C=	ENSP00000508017.1:n.469-87C=
ENST00000682659.1:c.541C=	ENSP00000507351.1:p.Arg181=
ENST00000682699.1:c.910C=	ENSP00000507935.1:p.Arg304=
ENST00000683237.1:c.*50C=	ENSP00000507343.1:n.*50C=
ENST00000683856.1:c.733C=	ENSP00000507979.1:p.Arg245=
ENST00000684006.1:c.*50C=	ENSP00000507269.1:n.*50C=
ENST00000684657.1:c.730C=	ENSP00000507961.1:p.Arg244=
XM_024448761.1:c.910C=	XP_024304529.1:p.Arg304=