Canonical Allele Identifier: CA1980172305
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490119C= , CM000673.2:g.67490119C= GRCh38
NC_000011.9:g.67257590C= , CM000673.1:g.67257590C= GRCh37
NC_000011.8:g.67014166C= NCBI36
NG_008969.1:g.12086C= , LRG_460:g.12086C=

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.527C=
ENST00000528641.7:c.361C= ENSP00000434982.3:p.Gln121=
ENST00000529797.2:n.1062C=
ENST00000682324.1:c.468+664C= ENSP00000508017.1:n.468+664C=
ENST00000682659.1:c.181C= ENSP00000507351.1:p.Gln61=
ENST00000682699.1:c.550C= ENSP00000507935.1:p.Gln184=
ENST00000683237.1:c.550C= ENSP00000507343.1:p.Gln184=
ENST00000683856.1:c.373C= ENSP00000507979.1:p.Gln125=
ENST00000684006.1:c.550C= ENSP00000507269.1:p.Gln184=
ENST00000684657.1:c.370C= ENSP00000507961.1:p.Gln124=
ENST00000279146.8:c.550C= MANE Select ENSP00000279146.3:p.Gln184=
ENST00000279146.7:c.550C= ENSP00000279146.3:p.Gln184=
ENST00000525341.1:c.202C= ENSP00000476993.1:p.Gln68=
ENST00000528641.6:c.361C= ENSP00000434982.2:p.Gln121=
NM_001302959.1:c.373C= NP_001289888.1:p.Gln125=
NM_001302960.1:c.550C= NP_001289889.1:p.Gln184=
NM_003977.3:c.550C= NP_003968.3:p.Gln184=
XM_024448761.1:c.550C= XP_024304529.1:p.Gln184=
NM_003977.4:c.550C= MANE Select NP_003968.3:p.Gln184=
NM_001302960.2:c.550C= NP_001289889.1:p.Gln184=
NM_001302959.2:c.373C= NP_001289888.1:p.Gln125=