Canonical Allele Identifier: CA2536050035

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67487101_67487102insCGGG , CM000673.2:g.67487101_67487102insCGGG	GRCh38
NC_000011.9:g.67254572_67254573insCGGG , CM000673.1:g.67254572_67254573insCGGG	GRCh37
NC_000011.8:g.67011148_67011149insCGGG	NCBI36
NG_008969.1:g.9068_9069insCGGG , LRG_460:g.9068_9069insCGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.172_173insCGGG
ENST00000528641.7:c.195_196insCGGG	ENSP00000434982.3:p.Lys66ArgfsTer27
ENST00000529797.2:n.125_126insCGGG
ENST00000682324.1:c.195_196insCGGG	ENSP00000508017.1:p.Lys66ArgfsTer27
ENST00000682659.1:c.100-2937_100-2936insCGGG	ENSP00000507351.1:n.100-2937_100-2936insCGGG
ENST00000682699.1:c.195_196insCGGG	ENSP00000507935.1:p.Lys66ArgfsTer27
ENST00000683237.1:c.195_196insCGGG	ENSP00000507343.1:p.Lys66ArgfsTer27
ENST00000683856.1:c.18_19insCGGG	ENSP00000507979.1:p.Lys7ArgfsTer27
ENST00000684006.1:c.195_196insCGGG	ENSP00000507269.1:p.Lys66ArgfsTer27
ENST00000684657.1:c.100-2166_100-2165insCGGG	ENSP00000507961.1:n.100-2166_100-2165insCGGG
ENST00000279146.8:c.195_196insCGGG MANE Select	ENSP00000279146.3:p.Lys66ArgfsTer27
ENST00000279146.7:c.195_196insCGGG	ENSP00000279146.3:p.Lys66ArgfsTer27
ENST00000528641.6:c.195_196insCGGG	ENSP00000434982.2:p.Lys66ArgfsTer27
ENST00000529797.1:n.305_306insCGGG
NM_001302959.1:c.18_19insCGGG	NP_001289888.1:p.Lys7ArgfsTer27
NM_001302960.1:c.195_196insCGGG	NP_001289889.1:p.Lys66ArgfsTer27
NM_003977.3:c.195_196insCGGG	NP_003968.3:p.Lys66ArgfsTer27
XM_024448761.1:c.195_196insCGGG	XP_024304529.1:p.Lys66ArgfsTer27
NM_003977.4:c.195_196insCGGG MANE Select	NP_003968.3:p.Lys66ArgfsTer27
NM_001302960.2:c.195_196insCGGG	NP_001289889.1:p.Lys66ArgfsTer27
NM_001302959.2:c.18_19insCGGG	NP_001289888.1:p.Lys7ArgfsTer27