Canonical Allele Identifier: CA1980170168

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67483196T= , CM000673.2:g.67483196T=	GRCh38
NC_000011.9:g.67250667T= , CM000673.1:g.67250667T=	GRCh37
NC_000011.8:g.67007243T=	NCBI36
NG_008969.1:g.5163T= , LRG_460:g.5163T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.15T=
ENST00000528641.7:c.38T=	ENSP00000434982.3:p.Ile13=
ENST00000682324.1:c.38T=	ENSP00000508017.1:p.Ile13=
ENST00000682659.1:c.38T=	ENSP00000507351.1:p.Ile13=
ENST00000682699.1:c.38T=	ENSP00000507935.1:p.Ile13=
ENST00000683237.1:c.38T=	ENSP00000507343.1:p.Ile13=
ENST00000684006.1:c.38T=	ENSP00000507269.1:p.Ile13=
ENST00000684657.1:c.38T=	ENSP00000507961.1:p.Ile13=
ENST00000279146.8:c.38T= MANE Select	ENSP00000279146.3:p.Ile13=
ENST00000279146.7:c.38T=	ENSP00000279146.3:p.Ile13=
ENST00000528641.6:c.38T=	ENSP00000434982.2:p.Ile13=
ENST00000529797.1:n.148T=
NM_001302960.1:c.38T=	NP_001289889.1:p.Ile13=
NM_003977.3:c.38T=	NP_003968.3:p.Ile13=
XM_024448761.1:c.38T=	XP_024304529.1:p.Ile13=
NM_003977.4:c.38T= MANE Select	NP_003968.3:p.Ile13=
NM_001302960.2:c.38T=	NP_001289889.1:p.Ile13=