Canonical Allele Identifier: CA2839589511

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490341del , CM000673.2:g.67490341del	GRCh38
NC_000011.9:g.67257812del , CM000673.1:g.67257812del	GRCh37
NC_000011.8:g.67014388del	NCBI36
NG_008969.1:g.12308del , LRG_460:g.12308del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.648del
ENST00000528641.7:c.482del	ENSP00000434982.3:p.Ile161ThrfsTer?
ENST00000529797.2:n.1183del
ENST00000682324.1:c.469-656del	ENSP00000508017.1:n.469-656del
ENST00000682659.1:c.302del	ENSP00000507351.1:p.Ile101ThrfsTer?
ENST00000682699.1:c.671del	ENSP00000507935.1:p.Ile224ThrfsTer?
ENST00000683237.1:c.671del	ENSP00000507343.1:p.Ile224ThrfsTer?
ENST00000683856.1:c.494del	ENSP00000507979.1:p.Ile165ThrfsTer?
ENST00000684006.1:c.671del	ENSP00000507269.1:p.Ile224ThrfsTer?
ENST00000684657.1:c.491del	ENSP00000507961.1:p.Ile164ThrfsTer?
ENST00000279146.8:c.671del MANE Select	ENSP00000279146.3:p.Ile224ThrfsTer?
ENST00000279146.7:c.671del	ENSP00000279146.3:p.Ile224ThrfsTer?
ENST00000525341.1:c.323del	ENSP00000476993.1:p.Ile108ThrfsTer?
ENST00000528641.6:c.482del	ENSP00000434982.2:p.Ile161ThrfsTer?
NM_001302959.1:c.494del	NP_001289888.1:p.Ile165ThrfsTer?
NM_001302960.1:c.671del	NP_001289889.1:p.Ile224ThrfsTer?
NM_003977.3:c.671del	NP_003968.3:p.Ile224ThrfsTer?
XM_024448761.1:c.671del	XP_024304529.1:p.Ile224ThrfsTer?
NM_003977.4:c.671del MANE Select	NP_003968.3:p.Ile224ThrfsTer?
NM_001302960.2:c.671del	NP_001289889.1:p.Ile224ThrfsTer?
NM_001302959.2:c.494del	NP_001289888.1:p.Ile165ThrfsTer?