Canonical Allele Identifier: CA1980172497

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490496G= , CM000673.2:g.67490496G=	GRCh38
NC_000011.9:g.67257967G= , CM000673.1:g.67257967G=	GRCh37
NC_000011.8:g.67014543G=	NCBI36
NG_008969.1:g.12463G= , LRG_460:g.12463G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.803G=
ENST00000528641.7:c.598+39G=	ENSP00000434982.3:n.598+39G=
ENST00000529797.2:n.1338G=
ENST00000682324.1:c.469-501G=	ENSP00000508017.1:n.469-501G=
ENST00000682659.1:c.418+39G=	ENSP00000507351.1:n.418+39G=
ENST00000682699.1:c.787+39G=	ENSP00000507935.1:n.787+39G=
ENST00000683237.1:c.779+47G=	ENSP00000507343.1:n.779+47G=
ENST00000683856.1:c.610+39G=	ENSP00000507979.1:n.610+39G=
ENST00000684006.1:c.787+39G=	ENSP00000507269.1:n.787+39G=
ENST00000684657.1:c.607+39G=	ENSP00000507961.1:n.607+39G=
ENST00000279146.8:c.787+39G= MANE Select	ENSP00000279146.3:n.787+39G=
ENST00000279146.7:c.787+39G=	ENSP00000279146.3:n.787+39G=
ENST00000525341.1:c.478G=	ENSP00000476993.1:p.Val160=
ENST00000528641.6:c.598+39G=	ENSP00000434982.2:n.598+39G=
NM_001302959.1:c.610+39G=	NP_001289888.1:n.610+39G=
NM_001302960.1:c.779+47G=	NP_001289889.1:n.779+47G=
NM_003977.3:c.787+39G=	NP_003968.3:n.787+39G=
XM_024448761.1:c.787+39G=	XP_024304529.1:n.787+39G=
NM_003977.4:c.787+39G= MANE Select	NP_003968.3:n.787+39G=
NM_001302960.2:c.779+47G=	NP_001289889.1:n.779+47G=
NM_001302959.2:c.610+39G=	NP_001289888.1:n.610+39G=