Canonical Allele Identifier: CA2832563237

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489423dup , CM000673.2:g.67489423dup	GRCh38
NC_000011.9:g.67256894dup , CM000673.1:g.67256894dup	GRCh37
NC_000011.8:g.67013470dup	NCBI36
NG_008969.1:g.11390dup , LRG_460:g.11390dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.413dup
ENST00000528641.7:c.280-615dup	ENSP00000434982.3:n.280-615dup
ENST00000529797.2:n.366dup
ENST00000682324.1:c.436dup	ENSP00000508017.1:p.Gln146ProfsTer?
ENST00000682659.1:c.100-615dup	ENSP00000507351.1:n.100-615dup
ENST00000682699.1:c.436dup	ENSP00000507935.1:p.Gln146ProfsTer?
ENST00000683237.1:c.436dup	ENSP00000507343.1:p.Gln146ProfsTer?
ENST00000683856.1:c.259dup	ENSP00000507979.1:p.Gln87ProfsTer?
ENST00000684006.1:c.436dup	ENSP00000507269.1:p.Gln146ProfsTer?
ENST00000684657.1:c.256dup	ENSP00000507961.1:p.Gln86ProfsTer?
ENST00000279146.8:c.436dup MANE Select	ENSP00000279146.3:p.Gln146ProfsTer?
ENST00000279146.7:c.436dup	ENSP00000279146.3:p.Gln146ProfsTer?
ENST00000525341.1:c.88dup	ENSP00000476993.1:p.Gln30ProfsTer?
ENST00000528641.6:c.280-615dup	ENSP00000434982.2:n.280-615dup
ENST00000529797.1:n.546dup
NM_001302959.1:c.259dup	NP_001289888.1:p.Gln87ProfsTer?
NM_001302960.1:c.436dup	NP_001289889.1:p.Gln146ProfsTer?
NM_003977.3:c.436dup	NP_003968.3:p.Gln146ProfsTer?
XM_024448761.1:c.436dup	XP_024304529.1:p.Gln146ProfsTer?
NM_003977.4:c.436dup MANE Select	NP_003968.3:p.Gln146ProfsTer?
NM_001302960.2:c.436dup	NP_001289889.1:p.Gln146ProfsTer?
NM_001302959.2:c.259dup	NP_001289888.1:p.Gln87ProfsTer?