Canonical Allele Identifier: CA2839108726
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67487156dup , CM000673.2:g.67487156dup GRCh38
NC_000011.9:g.67254627dup , CM000673.1:g.67254627dup GRCh37
NC_000011.8:g.67011203dup NCBI36
NG_008969.1:g.9123dup , LRG_460:g.9123dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000525341.2:c.227dup
ENST00000528641.7:c.250dup ENSP00000434982.3:p.Glu84GlyfsTer8
ENST00000529797.2:n.180dup
ENST00000682324.1:c.250dup ENSP00000508017.1:p.Glu84GlyfsTer8
ENST00000682659.1:c.100-2882dup ENSP00000507351.1:n.100-2882dup
ENST00000682699.1:c.250dup ENSP00000507935.1:p.Glu84GlyfsTer8
ENST00000683237.1:c.250dup ENSP00000507343.1:p.Glu84GlyfsTer8
ENST00000683856.1:c.73dup ENSP00000507979.1:p.Glu25GlyfsTer8
ENST00000684006.1:c.250dup ENSP00000507269.1:p.Glu84GlyfsTer8
ENST00000684657.1:c.100-2111dup ENSP00000507961.1:n.100-2111dup
ENST00000279146.8:c.250dup MANE Select ENSP00000279146.3:p.Glu84GlyfsTer8
ENST00000279146.7:c.250dup ENSP00000279146.3:p.Glu84GlyfsTer8
ENST00000528641.6:c.250dup ENSP00000434982.2:p.Glu84GlyfsTer8
ENST00000529797.1:n.360dup
NM_001302959.1:c.73dup NP_001289888.1:p.Glu25GlyfsTer8
NM_001302960.1:c.250dup NP_001289889.1:p.Glu84GlyfsTer8
NM_003977.3:c.250dup NP_003968.3:p.Glu84GlyfsTer8
XM_024448761.1:c.250dup XP_024304529.1:p.Glu84GlyfsTer8
NM_003977.4:c.250dup MANE Select NP_003968.3:p.Glu84GlyfsTer8
NM_001302960.2:c.250dup NP_001289889.1:p.Glu84GlyfsTer8
NM_001302959.2:c.73dup NP_001289888.1:p.Glu25GlyfsTer8