Canonical Allele Identifier: CA1980172296

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490103A= , CM000673.2:g.67490103A=	GRCh38
NC_000011.9:g.67257574A= , CM000673.1:g.67257574A=	GRCh37
NC_000011.8:g.67014150A=	NCBI36
NG_008969.1:g.12070A= , LRG_460:g.12070A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.511A=
ENST00000528641.7:c.345A=	ENSP00000434982.3:p.Ala115=
ENST00000529797.2:n.1046A=
ENST00000682324.1:c.468+648A=	ENSP00000508017.1:n.468+648A=
ENST00000682659.1:c.165A=	ENSP00000507351.1:p.Ala55=
ENST00000682699.1:c.534A=	ENSP00000507935.1:p.Ala178=
ENST00000683237.1:c.534A=	ENSP00000507343.1:p.Ala178=
ENST00000683856.1:c.357A=	ENSP00000507979.1:p.Ala119=
ENST00000684006.1:c.534A=	ENSP00000507269.1:p.Ala178=
ENST00000684657.1:c.354A=	ENSP00000507961.1:p.Ala118=
ENST00000279146.8:c.534A= MANE Select	ENSP00000279146.3:p.Ala178=
ENST00000279146.7:c.534A=	ENSP00000279146.3:p.Ala178=
ENST00000525341.1:c.186A=	ENSP00000476993.1:p.Ala62=
ENST00000528641.6:c.345A=	ENSP00000434982.2:p.Ala115=
NM_001302959.1:c.357A=	NP_001289888.1:p.Ala119=
NM_001302960.1:c.534A=	NP_001289889.1:p.Ala178=
NM_003977.3:c.534A=	NP_003968.3:p.Ala178=
XM_024448761.1:c.534A=	XP_024304529.1:p.Ala178=
NM_003977.4:c.534A= MANE Select	NP_003968.3:p.Ala178=
NM_001302960.2:c.534A=	NP_001289889.1:p.Ala178=
NM_001302959.2:c.357A=	NP_001289888.1:p.Ala119=