Canonical Allele Identifier: CA224161267

Gene: AIP

Linked Data

• dbSNP Id: rs773531266
• MyVariant Identifiers: chr11:g.67250971_67250972insGGGTTG (hg19) ; chr11:g.67483500_67483501insGGGTTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67483510_67483515dup , CM000673.2:g.67483510_67483515dup	GRCh38
NC_000011.9:g.67250981_67250986dup , CM000673.1:g.67250981_67250986dup	GRCh37
NC_000011.8:g.67007557_67007562dup	NCBI36
NG_008969.1:g.5477_5482dup , LRG_460:g.5477_5482dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.76+253_76+258dup
ENST00000528641.7:c.99+253_99+258dup	ENSP00000434982.3:n.99+253_99+258dup
ENST00000529797.2:n.29+253_29+258dup
ENST00000682324.1:c.99+253_99+258dup	ENSP00000508017.1:n.99+253_99+258dup
ENST00000682659.1:c.99+253_99+258dup	ENSP00000507351.1:n.99+253_99+258dup
ENST00000682699.1:c.99+253_99+258dup	ENSP00000507935.1:n.99+253_99+258dup
ENST00000683237.1:c.99+253_99+258dup	ENSP00000507343.1:n.99+253_99+258dup
ENST00000683856.1:c.-279_-274dup	ENSP00000507979.1:n.-279_-274dup
ENST00000684006.1:c.99+253_99+258dup	ENSP00000507269.1:n.99+253_99+258dup
ENST00000684657.1:c.99+253_99+258dup	ENSP00000507961.1:n.99+253_99+258dup
ENST00000279146.8:c.99+253_99+258dup MANE Select	ENSP00000279146.3:n.99+253_99+258dup
ENST00000279146.7:c.99+253_99+258dup	ENSP00000279146.3:n.99+253_99+258dup
ENST00000528641.6:c.99+253_99+258dup	ENSP00000434982.2:n.99+253_99+258dup
ENST00000529797.1:n.209+253_209+258dup
NM_001302960.1:c.99+253_99+258dup	NP_001289889.1:n.99+253_99+258dup
NM_003977.3:c.99+253_99+258dup	NP_003968.3:n.99+253_99+258dup
XM_024448761.1:c.99+253_99+258dup	XP_024304529.1:n.99+253_99+258dup
NM_003977.4:c.99+253_99+258dup MANE Select	NP_003968.3:n.99+253_99+258dup
NM_001302960.2:c.99+253_99+258dup	NP_001289889.1:n.99+253_99+258dup