Canonical Allele Identifier: CA1980171971

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489391A= , CM000673.2:g.67489391A=	GRCh38
NC_000011.9:g.67256862A= , CM000673.1:g.67256862A=	GRCh37
NC_000011.8:g.67013438A=	NCBI36
NG_008969.1:g.11358A= , LRG_460:g.11358A=

Transcript Alleles

HGVS	Amino-acid Change
NM_003977.4:c.404A= MANE Select	NP_003968.3:p.His135=
ENST00000279146.8:c.404A= MANE Select	ENSP00000279146.3:p.His135=
NM_001302959.1:c.227A=	NP_001289888.1:p.His76=
NM_001302959.2:c.227A=	NP_001289888.1:p.His76=
NM_001302960.1:c.404A=	NP_001289889.1:p.His135=
NM_001302960.2:c.404A=	NP_001289889.1:p.His135=
NM_003977.3:c.404A=	NP_003968.3:p.His135=
ENST00000279146.7:c.404A=	ENSP00000279146.3:p.His135=
ENST00000525341.1:c.56A=	ENSP00000476993.1:p.His19=
ENST00000525341.2:c.381A=
ENST00000528641.6:c.280-647A=	ENSP00000434982.2:n.280-647A=
ENST00000528641.7:c.280-647A=	ENSP00000434982.3:n.280-647A=
ENST00000529797.1:n.514A=
ENST00000529797.2:n.334A=
ENST00000682324.1:c.404A=	ENSP00000508017.1:p.His135=
ENST00000682659.1:c.100-647A=	ENSP00000507351.1:n.100-647A=
ENST00000682699.1:c.404A=	ENSP00000507935.1:p.His135=
ENST00000683237.1:c.404A=	ENSP00000507343.1:p.His135=
ENST00000683856.1:c.227A=	ENSP00000507979.1:p.His76=
ENST00000684006.1:c.404A=	ENSP00000507269.1:p.His135=
ENST00000684657.1:c.224A=	ENSP00000507961.1:p.His75=
XM_024448761.1:c.404A=	XP_024304529.1:p.His135=