Canonical Allele Identifier: CA1980172643

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490804C= , CM000673.2:g.67490804C=	GRCh38
NC_000011.9:g.67258275C= , CM000673.1:g.67258275C=	GRCh37
NC_000011.8:g.67014851C=	NCBI36
NG_008969.1:g.12771C= , LRG_460:g.12771C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1111C=
ENST00000528641.7:c.615C=	ENSP00000434982.3:p.Tyr205=
ENST00000529797.2:n.1646C=
ENST00000682324.1:c.469-193C=	ENSP00000508017.1:n.469-193C=
ENST00000682659.1:c.435C=	ENSP00000507351.1:p.Tyr145=
ENST00000682699.1:c.804C=	ENSP00000507935.1:p.Tyr268=
ENST00000683237.1:c.796C=	ENSP00000507343.1:p.Leu266=
ENST00000683856.1:c.627C=	ENSP00000507979.1:p.Tyr209=
ENST00000684006.1:c.793C=	ENSP00000507269.1:p.Leu265=
ENST00000684657.1:c.624C=	ENSP00000507961.1:p.Tyr208=
ENST00000279146.8:c.804C= MANE Select	ENSP00000279146.3:p.Tyr268=
ENST00000279146.7:c.804C=	ENSP00000279146.3:p.Tyr268=
ENST00000528641.6:c.615C=	ENSP00000434982.2:p.Tyr205=
NM_001302959.1:c.627C=	NP_001289888.1:p.Tyr209=
NM_001302960.1:c.796C=	NP_001289889.1:p.Leu266=
NM_003977.3:c.804C=	NP_003968.3:p.Tyr268=
XM_024448761.1:c.804C=	XP_024304529.1:p.Tyr268=
NM_003977.4:c.804C= MANE Select	NP_003968.3:p.Tyr268=
NM_001302960.2:c.796C=	NP_001289889.1:p.Leu266=
NM_001302959.2:c.627C=	NP_001289888.1:p.Tyr209=