Canonical Allele Identifier: CA1980172406

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490328T= , CM000673.2:g.67490328T=	GRCh38
NC_000011.9:g.67257799T= , CM000673.1:g.67257799T=	GRCh37
NC_000011.8:g.67014375T=	NCBI36
NG_008969.1:g.12295T= , LRG_460:g.12295T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.635T=
ENST00000528641.7:c.469T=	ENSP00000434982.3:p.Ser157=
ENST00000529797.2:n.1170T=
ENST00000682324.1:c.469-669T=	ENSP00000508017.1:n.469-669T=
ENST00000682659.1:c.289T=	ENSP00000507351.1:p.Ser97=
ENST00000682699.1:c.658T=	ENSP00000507935.1:p.Ser220=
ENST00000683237.1:c.658T=	ENSP00000507343.1:p.Ser220=
ENST00000683856.1:c.481T=	ENSP00000507979.1:p.Ser161=
ENST00000684006.1:c.658T=	ENSP00000507269.1:p.Ser220=
ENST00000684657.1:c.478T=	ENSP00000507961.1:p.Ser160=
ENST00000279146.8:c.658T= MANE Select	ENSP00000279146.3:p.Ser220=
ENST00000279146.7:c.658T=	ENSP00000279146.3:p.Ser220=
ENST00000525341.1:c.310T=	ENSP00000476993.1:p.Ser104=
ENST00000528641.6:c.469T=	ENSP00000434982.2:p.Ser157=
NM_001302959.1:c.481T=	NP_001289888.1:p.Ser161=
NM_001302960.1:c.658T=	NP_001289889.1:p.Ser220=
NM_003977.3:c.658T=	NP_003968.3:p.Ser220=
XM_024448761.1:c.658T=	XP_024304529.1:p.Ser220=
NM_003977.4:c.658T= MANE Select	NP_003968.3:p.Ser220=
NM_001302960.2:c.658T=	NP_001289889.1:p.Ser220=
NM_001302959.2:c.481T=	NP_001289888.1:p.Ser161=