Canonical Allele Identifier: CA1980172308
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490126G= , CM000673.2:g.67490126G= GRCh38
NC_000011.9:g.67257597G= , CM000673.1:g.67257597G= GRCh37
NC_000011.8:g.67014173G= NCBI36
NG_008969.1:g.12093G= , LRG_460:g.12093G=

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.534G=
ENST00000528641.7:c.368G= ENSP00000434982.3:p.Gly123=
ENST00000529797.2:n.1069G=
ENST00000682324.1:c.468+671G= ENSP00000508017.1:n.468+671G=
ENST00000682659.1:c.188G= ENSP00000507351.1:p.Gly63=
ENST00000682699.1:c.557G= ENSP00000507935.1:p.Gly186=
ENST00000683237.1:c.557G= ENSP00000507343.1:p.Gly186=
ENST00000683856.1:c.380G= ENSP00000507979.1:p.Gly127=
ENST00000684006.1:c.557G= ENSP00000507269.1:p.Gly186=
ENST00000684657.1:c.377G= ENSP00000507961.1:p.Gly126=
ENST00000279146.8:c.557G= MANE Select ENSP00000279146.3:p.Gly186=
ENST00000279146.7:c.557G= ENSP00000279146.3:p.Gly186=
ENST00000525341.1:c.209G= ENSP00000476993.1:p.Gly70=
ENST00000528641.6:c.368G= ENSP00000434982.2:p.Gly123=
NM_001302959.1:c.380G= NP_001289888.1:p.Gly127=
NM_001302960.1:c.557G= NP_001289889.1:p.Gly186=
NM_003977.3:c.557G= NP_003968.3:p.Gly186=
XM_024448761.1:c.557G= XP_024304529.1:p.Gly186=
NM_003977.4:c.557G= MANE Select NP_003968.3:p.Gly186=
NM_001302960.2:c.557G= NP_001289889.1:p.Gly186=
NM_001302959.2:c.380G= NP_001289888.1:p.Gly127=