Canonical Allele Identifier: CA1980172339

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490189C= , CM000673.2:g.67490189C=	GRCh38
NC_000011.9:g.67257660C= , CM000673.1:g.67257660C=	GRCh37
NC_000011.8:g.67014236C=	NCBI36
NG_008969.1:g.12156C= , LRG_460:g.12156C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.597C=
ENST00000528641.7:c.431C=	ENSP00000434982.3:p.Ala144=
ENST00000529797.2:n.1132C=
ENST00000682324.1:c.468+734C=	ENSP00000508017.1:n.468+734C=
ENST00000682659.1:c.251C=	ENSP00000507351.1:p.Ala84=
ENST00000682699.1:c.620C=	ENSP00000507935.1:p.Ala207=
ENST00000683237.1:c.620C=	ENSP00000507343.1:p.Ala207=
ENST00000683856.1:c.443C=	ENSP00000507979.1:p.Ala148=
ENST00000684006.1:c.620C=	ENSP00000507269.1:p.Ala207=
ENST00000684657.1:c.440C=	ENSP00000507961.1:p.Ala147=
ENST00000279146.8:c.620C= MANE Select	ENSP00000279146.3:p.Ala207=
ENST00000279146.7:c.620C=	ENSP00000279146.3:p.Ala207=
ENST00000525341.1:c.272C=	ENSP00000476993.1:p.Ala91=
ENST00000528641.6:c.431C=	ENSP00000434982.2:p.Ala144=
NM_001302959.1:c.443C=	NP_001289888.1:p.Ala148=
NM_001302960.1:c.620C=	NP_001289889.1:p.Ala207=
NM_003977.3:c.620C=	NP_003968.3:p.Ala207=
XM_024448761.1:c.620C=	XP_024304529.1:p.Ala207=
NM_003977.4:c.620C= MANE Select	NP_003968.3:p.Ala207=
NM_001302960.2:c.620C=	NP_001289889.1:p.Ala207=
NM_001302959.2:c.443C=	NP_001289888.1:p.Ala148=