Canonical Allele Identifier: CA1980170878
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67486979T= , CM000673.2:g.67486979T= GRCh38
NC_000011.9:g.67254450T= , CM000673.1:g.67254450T= GRCh37
NC_000011.8:g.67011026T= NCBI36
NG_008969.1:g.8946T= , LRG_460:g.8946T=

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.77-27T=
ENST00000528641.7:c.100-27T= ENSP00000434982.3:n.100-27T=
ENST00000529797.2:n.30-27T=
ENST00000682324.1:c.100-27T= ENSP00000508017.1:n.100-27T=
ENST00000682659.1:c.100-3059T= ENSP00000507351.1:n.100-3059T=
ENST00000682699.1:c.100-27T= ENSP00000507935.1:n.100-27T=
ENST00000683237.1:c.100-27T= ENSP00000507343.1:n.100-27T=
ENST00000683856.1:c.-78-27T= ENSP00000507979.1:n.-78-27T=
ENST00000684006.1:c.100-27T= ENSP00000507269.1:n.100-27T=
ENST00000684657.1:c.100-2288T= ENSP00000507961.1:n.100-2288T=
ENST00000279146.8:c.100-27T= MANE Select ENSP00000279146.3:n.100-27T=
ENST00000279146.7:c.100-27T= ENSP00000279146.3:n.100-27T=
ENST00000528641.6:c.100-27T= ENSP00000434982.2:n.100-27T=
ENST00000529797.1:n.210-27T=
NM_001302959.1:c.-78-27T= NP_001289888.1:n.-78-27T=
NM_001302960.1:c.100-27T= NP_001289889.1:n.100-27T=
NM_003977.3:c.100-27T= NP_003968.3:n.100-27T=
XM_024448761.1:c.100-27T= XP_024304529.1:n.100-27T=
NM_003977.4:c.100-27T= MANE Select NP_003968.3:n.100-27T=
NM_001302960.2:c.100-27T= NP_001289889.1:n.100-27T=
NM_001302959.2:c.-78-27T= NP_001289888.1:n.-78-27T=