Canonical Allele Identifier: CA2574896183
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67483251del , CM000673.2:g.67483251del GRCh38
NC_000011.9:g.67250722del , CM000673.1:g.67250722del GRCh37
NC_000011.8:g.67007298del NCBI36
NG_008969.1:g.5218del , LRG_460:g.5218del

Transcript Alleles

HGVS Amino-acid Change
ENST00000525341.2:c.70del
ENST00000528641.7:c.93del ENSP00000434982.3:p.Thr32ProfsTer?
ENST00000529797.2:n.23del
ENST00000682324.1:c.93del ENSP00000508017.1:p.Thr32ProfsTer?
ENST00000682659.1:c.93del ENSP00000507351.1:p.Thr32ProfsTer16
ENST00000682699.1:c.93del ENSP00000507935.1:p.Thr32ProfsTer?
ENST00000683237.1:c.93del ENSP00000507343.1:p.Thr32ProfsTer?
ENST00000684006.1:c.93del ENSP00000507269.1:p.Thr32ProfsTer?
ENST00000684657.1:c.93del ENSP00000507961.1:p.Thr32ProfsTer?
ENST00000279146.8:c.93del MANE Select ENSP00000279146.3:p.Thr32ProfsTer?
ENST00000279146.7:c.93del ENSP00000279146.3:p.Thr32ProfsTer?
ENST00000528641.6:c.93del ENSP00000434982.2:p.Thr32ProfsTer?
ENST00000529797.1:n.203del
NM_001302960.1:c.93del NP_001289889.1:p.Thr32ProfsTer?
NM_003977.3:c.93del NP_003968.3:p.Thr32ProfsTer?
XM_024448761.1:c.93del XP_024304529.1:p.Thr32ProfsTer?
NM_003977.4:c.93del MANE Select NP_003968.3:p.Thr32ProfsTer?
NM_001302960.2:c.93del NP_001289889.1:p.Thr32ProfsTer?