Canonical Allele Identifier: CA1980172281

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490070A= , CM000673.2:g.67490070A=	GRCh38
NC_000011.9:g.67257541A= , CM000673.1:g.67257541A=	GRCh37
NC_000011.8:g.67014117A=	NCBI36
NG_008969.1:g.12037A= , LRG_460:g.12037A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.478A=
ENST00000528641.7:c.312A=	ENSP00000434982.3:p.Pro104=
ENST00000529797.2:n.1013A=
ENST00000682324.1:c.468+615A=	ENSP00000508017.1:n.468+615A=
ENST00000682659.1:c.132A=	ENSP00000507351.1:p.Pro44=
ENST00000682699.1:c.501A=	ENSP00000507935.1:p.Pro167=
ENST00000683237.1:c.501A=	ENSP00000507343.1:p.Pro167=
ENST00000683856.1:c.324A=	ENSP00000507979.1:p.Pro108=
ENST00000684006.1:c.501A=	ENSP00000507269.1:p.Pro167=
ENST00000684657.1:c.321A=	ENSP00000507961.1:p.Pro107=
ENST00000279146.8:c.501A= MANE Select	ENSP00000279146.3:p.Pro167=
ENST00000279146.7:c.501A=	ENSP00000279146.3:p.Pro167=
ENST00000525341.1:c.153A=	ENSP00000476993.1:p.Pro51=
ENST00000528641.6:c.312A=	ENSP00000434982.2:p.Pro104=
NM_001302959.1:c.324A=	NP_001289888.1:p.Pro108=
NM_001302960.1:c.501A=	NP_001289889.1:p.Pro167=
NM_003977.3:c.501A=	NP_003968.3:p.Pro167=
XM_024448761.1:c.501A=	XP_024304529.1:p.Pro167=
NM_003977.4:c.501A= MANE Select	NP_003968.3:p.Pro167=
NM_001302960.2:c.501A=	NP_001289889.1:p.Pro167=
NM_001302959.2:c.324A=	NP_001289888.1:p.Pro108=