Canonical Allele Identifier: CA1980172407

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490329C= , CM000673.2:g.67490329C=	GRCh38
NC_000011.9:g.67257800C= , CM000673.1:g.67257800C=	GRCh37
NC_000011.8:g.67014376C=	NCBI36
NG_008969.1:g.12296C= , LRG_460:g.12296C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.636C=
ENST00000528641.7:c.470C=	ENSP00000434982.3:p.Ser157=
ENST00000529797.2:n.1171C=
ENST00000682324.1:c.469-668C=	ENSP00000508017.1:n.469-668C=
ENST00000682659.1:c.290C=	ENSP00000507351.1:p.Ser97=
ENST00000682699.1:c.659C=	ENSP00000507935.1:p.Ser220=
ENST00000683237.1:c.659C=	ENSP00000507343.1:p.Ser220=
ENST00000683856.1:c.482C=	ENSP00000507979.1:p.Ser161=
ENST00000684006.1:c.659C=	ENSP00000507269.1:p.Ser220=
ENST00000684657.1:c.479C=	ENSP00000507961.1:p.Ser160=
ENST00000279146.8:c.659C= MANE Select	ENSP00000279146.3:p.Ser220=
ENST00000279146.7:c.659C=	ENSP00000279146.3:p.Ser220=
ENST00000525341.1:c.311C=	ENSP00000476993.1:p.Ser104=
ENST00000528641.6:c.470C=	ENSP00000434982.2:p.Ser157=
NM_001302959.1:c.482C=	NP_001289888.1:p.Ser161=
NM_001302960.1:c.659C=	NP_001289889.1:p.Ser220=
NM_003977.3:c.659C=	NP_003968.3:p.Ser220=
XM_024448761.1:c.659C=	XP_024304529.1:p.Ser220=
NM_003977.4:c.659C= MANE Select	NP_003968.3:p.Ser220=
NM_001302960.2:c.659C=	NP_001289889.1:p.Ser220=
NM_001302959.2:c.482C=	NP_001289888.1:p.Ser161=