Canonical Allele Identifier: CA1980172424

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490366G= , CM000673.2:g.67490366G=	GRCh38
NC_000011.9:g.67257837G= , CM000673.1:g.67257837G=	GRCh37
NC_000011.8:g.67014413G=	NCBI36
NG_008969.1:g.12333G= , LRG_460:g.12333G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.673G=
ENST00000528641.7:c.507G=	ENSP00000434982.3:p.Pro169=
ENST00000529797.2:n.1208G=
ENST00000682324.1:c.469-631G=	ENSP00000508017.1:n.469-631G=
ENST00000682659.1:c.327G=	ENSP00000507351.1:p.Pro109=
ENST00000682699.1:c.696G=	ENSP00000507935.1:p.Pro232=
ENST00000683237.1:c.696G=	ENSP00000507343.1:p.Pro232=
ENST00000683856.1:c.519G=	ENSP00000507979.1:p.Pro173=
ENST00000684006.1:c.696G=	ENSP00000507269.1:p.Pro232=
ENST00000684657.1:c.516G=	ENSP00000507961.1:p.Pro172=
ENST00000279146.8:c.696G= MANE Select	ENSP00000279146.3:p.Pro232=
ENST00000279146.7:c.696G=	ENSP00000279146.3:p.Pro232=
ENST00000525341.1:c.348G=	ENSP00000476993.1:p.Pro116=
ENST00000528641.6:c.507G=	ENSP00000434982.2:p.Pro169=
NM_001302959.1:c.519G=	NP_001289888.1:p.Pro173=
NM_001302960.1:c.696G=	NP_001289889.1:p.Pro232=
NM_003977.3:c.696G=	NP_003968.3:p.Pro232=
XM_024448761.1:c.696G=	XP_024304529.1:p.Pro232=
NM_003977.4:c.696G= MANE Select	NP_003968.3:p.Pro232=
NM_001302960.2:c.696G=	NP_001289889.1:p.Pro232=
NM_001302959.2:c.519G=	NP_001289888.1:p.Pro173=