Canonical Allele Identifier: CA1980172670
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490862T= , CM000673.2:g.67490862T= GRCh38
NC_000011.9:g.67258333T= , CM000673.1:g.67258333T= GRCh37
NC_000011.8:g.67014909T= NCBI36
NG_008969.1:g.12829T= , LRG_460:g.12829T=

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.1169T=
ENST00000528641.7:c.673T= ENSP00000434982.3:p.Phe225=
ENST00000529797.2:n.1704T=
ENST00000682324.1:c.469-135T= ENSP00000508017.1:n.469-135T=
ENST00000682659.1:c.493T= ENSP00000507351.1:p.Phe165=
ENST00000682699.1:c.862T= ENSP00000507935.1:p.Phe288=
ENST00000683237.1:c.*2T= ENSP00000507343.1:n.*2T=
ENST00000683856.1:c.685T= ENSP00000507979.1:p.Phe229=
ENST00000684006.1:c.*2T= ENSP00000507269.1:n.*2T=
ENST00000684657.1:c.682T= ENSP00000507961.1:p.Phe228=
ENST00000279146.8:c.862T= MANE Select ENSP00000279146.3:p.Phe288=
ENST00000279146.7:c.862T= ENSP00000279146.3:p.Phe288=
ENST00000528641.6:c.673T= ENSP00000434982.2:p.Phe225=
NM_001302959.1:c.685T= NP_001289888.1:p.Phe229=
NM_001302960.1:c.*2T= NP_001289889.1:n.*2T=
NM_003977.3:c.862T= NP_003968.3:p.Phe288=
XM_024448761.1:c.862T= XP_024304529.1:p.Phe288=
NM_003977.4:c.862T= MANE Select NP_003968.3:p.Phe288=
NM_001302960.2:c.*2T= NP_001289889.1:n.*2T=
NM_001302959.2:c.685T= NP_001289888.1:p.Phe229=