Canonical Allele Identifier: CA1980172315

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490140C= , CM000673.2:g.67490140C=	GRCh38
NC_000011.9:g.67257611C= , CM000673.1:g.67257611C=	GRCh37
NC_000011.8:g.67014187C=	NCBI36
NG_008969.1:g.12107C= , LRG_460:g.12107C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.548C=
ENST00000528641.7:c.382C=	ENSP00000434982.3:p.Arg128=
ENST00000529797.2:n.1083C=
ENST00000682324.1:c.468+685C=	ENSP00000508017.1:n.468+685C=
ENST00000682659.1:c.202C=	ENSP00000507351.1:p.Arg68=
ENST00000682699.1:c.571C=	ENSP00000507935.1:p.Arg191=
ENST00000683237.1:c.571C=	ENSP00000507343.1:p.Arg191=
ENST00000683856.1:c.394C=	ENSP00000507979.1:p.Arg132=
ENST00000684006.1:c.571C=	ENSP00000507269.1:p.Arg191=
ENST00000684657.1:c.391C=	ENSP00000507961.1:p.Arg131=
ENST00000279146.8:c.571C= MANE Select	ENSP00000279146.3:p.Arg191=
ENST00000279146.7:c.571C=	ENSP00000279146.3:p.Arg191=
ENST00000525341.1:c.223C=	ENSP00000476993.1:p.Arg75=
ENST00000528641.6:c.382C=	ENSP00000434982.2:p.Arg128=
NM_001302959.1:c.394C=	NP_001289888.1:p.Arg132=
NM_001302960.1:c.571C=	NP_001289889.1:p.Arg191=
NM_003977.3:c.571C=	NP_003968.3:p.Arg191=
XM_024448761.1:c.571C=	XP_024304529.1:p.Arg191=
NM_003977.4:c.571C= MANE Select	NP_003968.3:p.Arg191=
NM_001302960.2:c.571C=	NP_001289889.1:p.Arg191=
NM_001302959.2:c.394C=	NP_001289888.1:p.Arg132=