Canonical Allele Identifier: CA1980172496

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490495G= , CM000673.2:g.67490495G=	GRCh38
NC_000011.9:g.67257966G= , CM000673.1:g.67257966G=	GRCh37
NC_000011.8:g.67014542G=	NCBI36
NG_008969.1:g.12462G= , LRG_460:g.12462G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.802G=
ENST00000528641.7:c.598+38G=	ENSP00000434982.3:n.598+38G=
ENST00000529797.2:n.1337G=
ENST00000682324.1:c.469-502G=	ENSP00000508017.1:n.469-502G=
ENST00000682659.1:c.418+38G=	ENSP00000507351.1:n.418+38G=
ENST00000682699.1:c.787+38G=	ENSP00000507935.1:n.787+38G=
ENST00000683237.1:c.779+46G=	ENSP00000507343.1:n.779+46G=
ENST00000683856.1:c.610+38G=	ENSP00000507979.1:n.610+38G=
ENST00000684006.1:c.787+38G=	ENSP00000507269.1:n.787+38G=
ENST00000684657.1:c.607+38G=	ENSP00000507961.1:n.607+38G=
ENST00000279146.8:c.787+38G= MANE Select	ENSP00000279146.3:n.787+38G=
ENST00000279146.7:c.787+38G=	ENSP00000279146.3:n.787+38G=
ENST00000525341.1:c.477G=	ENSP00000476993.1:p.Val159=
ENST00000528641.6:c.598+38G=	ENSP00000434982.2:n.598+38G=
NM_001302959.1:c.610+38G=	NP_001289888.1:n.610+38G=
NM_001302960.1:c.779+46G=	NP_001289889.1:n.779+46G=
NM_003977.3:c.787+38G=	NP_003968.3:n.787+38G=
XM_024448761.1:c.787+38G=	XP_024304529.1:n.787+38G=
NM_003977.4:c.787+38G= MANE Select	NP_003968.3:n.787+38G=
NM_001302960.2:c.779+46G=	NP_001289889.1:n.779+46G=
NM_001302959.2:c.610+38G=	NP_001289888.1:n.610+38G=