Canonical Allele Identifier: CA1980170169

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67483197C= , CM000673.2:g.67483197C=	GRCh38
NC_000011.9:g.67250668C= , CM000673.1:g.67250668C=	GRCh37
NC_000011.8:g.67007244C=	NCBI36
NG_008969.1:g.5164C= , LRG_460:g.5164C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.16C=
ENST00000528641.7:c.39C=	ENSP00000434982.3:p.Ile13=
ENST00000682324.1:c.39C=	ENSP00000508017.1:p.Ile13=
ENST00000682659.1:c.39C=	ENSP00000507351.1:p.Ile13=
ENST00000682699.1:c.39C=	ENSP00000507935.1:p.Ile13=
ENST00000683237.1:c.39C=	ENSP00000507343.1:p.Ile13=
ENST00000684006.1:c.39C=	ENSP00000507269.1:p.Ile13=
ENST00000684657.1:c.39C=	ENSP00000507961.1:p.Ile13=
ENST00000279146.8:c.39C= MANE Select	ENSP00000279146.3:p.Ile13=
ENST00000279146.7:c.39C=	ENSP00000279146.3:p.Ile13=
ENST00000528641.6:c.39C=	ENSP00000434982.2:p.Ile13=
ENST00000529797.1:n.149C=
NM_001302960.1:c.39C=	NP_001289889.1:p.Ile13=
NM_003977.3:c.39C=	NP_003968.3:p.Ile13=
XM_024448761.1:c.39C=	XP_024304529.1:p.Ile13=
NM_003977.4:c.39C= MANE Select	NP_003968.3:p.Ile13=
NM_001302960.2:c.39C=	NP_001289889.1:p.Ile13=