Canonical Allele Identifier: CA2839745831
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490845dup , CM000673.2:g.67490845dup GRCh38
NC_000011.9:g.67258316dup , CM000673.1:g.67258316dup GRCh37
NC_000011.8:g.67014892dup NCBI36
NG_008969.1:g.12812dup , LRG_460:g.12812dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000525341.2:c.1152dup
ENST00000528641.7:c.656dup ENSP00000434982.3:p.Glu220GlyfsTer5
ENST00000529797.2:n.1687dup
ENST00000682324.1:c.469-152dup ENSP00000508017.1:n.469-152dup
ENST00000682659.1:c.476dup ENSP00000507351.1:p.Glu160GlyfsTer5
ENST00000682699.1:c.845dup ENSP00000507935.1:p.Glu283GlyfsTer5
ENST00000683237.1:c.837dup ENSP00000507343.1:p.Gly280ArgfsTer21
ENST00000683856.1:c.668dup ENSP00000507979.1:p.Glu224GlyfsTer5
ENST00000684006.1:c.834dup ENSP00000507269.1:p.Gly279ArgfsTer21
ENST00000684657.1:c.665dup ENSP00000507961.1:p.Glu223GlyfsTer5
ENST00000279146.8:c.845dup MANE Select ENSP00000279146.3:p.Glu283GlyfsTer5
ENST00000279146.7:c.845dup ENSP00000279146.3:p.Glu283GlyfsTer5
ENST00000528641.6:c.656dup ENSP00000434982.2:p.Glu220GlyfsTer5
NM_001302959.1:c.668dup NP_001289888.1:p.Glu224GlyfsTer5
NM_001302960.1:c.837dup NP_001289889.1:p.Gly280ArgfsTer21
NM_003977.3:c.845dup NP_003968.3:p.Glu283GlyfsTer5
XM_024448761.1:c.845dup XP_024304529.1:p.Glu283GlyfsTer5
NM_003977.4:c.845dup MANE Select NP_003968.3:p.Glu283GlyfsTer5
NM_001302960.2:c.837dup NP_001289889.1:p.Gly280ArgfsTer21
NM_001302959.2:c.668dup NP_001289888.1:p.Glu224GlyfsTer5