Canonical Allele Identifier: CA2525229818
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67487096_67487099del , CM000673.2:g.67487096_67487099del GRCh38
NC_000011.9:g.67254567_67254570del , CM000673.1:g.67254567_67254570del GRCh37
NC_000011.8:g.67011143_67011146del NCBI36
NG_008969.1:g.9063_9066del , LRG_460:g.9063_9066del

Transcript Alleles

HGVS Amino-acid Change
ENST00000525341.2:c.167_170del
ENST00000528641.7:c.190_193del ENSP00000434982.3:p.Ile64AlafsTer?
ENST00000529797.2:n.120_123del
ENST00000682324.1:c.190_193del ENSP00000508017.1:p.Ile64AlafsTer?
ENST00000682659.1:c.100-2942_100-2939del ENSP00000507351.1:n.100-2942_100-2939del
ENST00000682699.1:c.190_193del ENSP00000507935.1:p.Ile64AlafsTer?
ENST00000683237.1:c.190_193del ENSP00000507343.1:p.Ile64AlafsTer?
ENST00000683856.1:c.13_16del ENSP00000507979.1:p.Ile5AlafsTer?
ENST00000684006.1:c.190_193del ENSP00000507269.1:p.Ile64AlafsTer?
ENST00000684657.1:c.100-2171_100-2168del ENSP00000507961.1:n.100-2171_100-2168del
ENST00000279146.8:c.190_193del MANE Select ENSP00000279146.3:p.Ile64AlafsTer?
ENST00000279146.7:c.190_193del ENSP00000279146.3:p.Ile64AlafsTer?
ENST00000528641.6:c.190_193del ENSP00000434982.2:p.Ile64AlafsTer?
ENST00000529797.1:n.300_303del
NM_001302959.1:c.13_16del NP_001289888.1:p.Ile5AlafsTer?
NM_001302960.1:c.190_193del NP_001289889.1:p.Ile64AlafsTer?
NM_003977.3:c.190_193del NP_003968.3:p.Ile64AlafsTer?
XM_024448761.1:c.190_193del XP_024304529.1:p.Ile64AlafsTer?
NM_003977.4:c.190_193del MANE Select NP_003968.3:p.Ile64AlafsTer?
NM_001302960.2:c.190_193del NP_001289889.1:p.Ile64AlafsTer?
NM_001302959.2:c.13_16del NP_001289888.1:p.Ile5AlafsTer?