Canonical Allele Identifier: CA1980170960

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67487147C= , CM000673.2:g.67487147C=	GRCh38
NC_000011.9:g.67254618C= , CM000673.1:g.67254618C=	GRCh37
NC_000011.8:g.67011194C=	NCBI36
NG_008969.1:g.9114C= , LRG_460:g.9114C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.218C=
ENST00000528641.7:c.241C=	ENSP00000434982.3:p.Arg81=
ENST00000529797.2:n.171C=
ENST00000682324.1:c.241C=	ENSP00000508017.1:p.Arg81=
ENST00000682659.1:c.100-2891C=	ENSP00000507351.1:n.100-2891C=
ENST00000682699.1:c.241C=	ENSP00000507935.1:p.Arg81=
ENST00000683237.1:c.241C=	ENSP00000507343.1:p.Arg81=
ENST00000683856.1:c.64C=	ENSP00000507979.1:p.Arg22=
ENST00000684006.1:c.241C=	ENSP00000507269.1:p.Arg81=
ENST00000684657.1:c.100-2120C=	ENSP00000507961.1:n.100-2120C=
ENST00000279146.8:c.241C= MANE Select	ENSP00000279146.3:p.Arg81=
ENST00000279146.7:c.241C=	ENSP00000279146.3:p.Arg81=
ENST00000528641.6:c.241C=	ENSP00000434982.2:p.Arg81=
ENST00000529797.1:n.351C=
NM_001302959.1:c.64C=	NP_001289888.1:p.Arg22=
NM_001302960.1:c.241C=	NP_001289889.1:p.Arg81=
NM_003977.3:c.241C=	NP_003968.3:p.Arg81=
XM_024448761.1:c.241C=	XP_024304529.1:p.Arg81=
NM_003977.4:c.241C= MANE Select	NP_003968.3:p.Arg81=
NM_001302960.2:c.241C=	NP_001289889.1:p.Arg81=
NM_001302959.2:c.64C=	NP_001289888.1:p.Arg22=