Canonical Allele Identifier: CA1980172279

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490066_67490067delinsAC , CM000673.2:g.67490066_67490067delinsAC	GRCh38
NC_000011.9:g.67257537_67257538delinsAC , CM000673.1:g.67257537_67257538delinsAC	GRCh37
NC_000011.8:g.67014113_67014114delinsAC	NCBI36
NG_008969.1:g.12033_12034delinsAC , LRG_460:g.12033_12034delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.474_475delinsAC
ENST00000528641.7:c.308_309delinsAC	ENSP00000434982.3:p.Asp103=
ENST00000529797.2:n.1009_1010delinsAC
ENST00000682324.1:c.468+611_468+612delinsAC	ENSP00000508017.1:n.468+611_468+612delinsAC
ENST00000682659.1:c.128_129delinsAC	ENSP00000507351.1:p.Asp43=
ENST00000682699.1:c.497_498delinsAC	ENSP00000507935.1:p.Asp166=
ENST00000683237.1:c.497_498delinsAC	ENSP00000507343.1:p.Asp166=
ENST00000683856.1:c.320_321delinsAC	ENSP00000507979.1:p.Asp107=
ENST00000684006.1:c.497_498delinsAC	ENSP00000507269.1:p.Asp166=
ENST00000684657.1:c.317_318delinsAC	ENSP00000507961.1:p.Asp106=
ENST00000279146.8:c.497_498delinsAC MANE Select	ENSP00000279146.3:p.Asp166=
ENST00000279146.7:c.497_498delinsAC	ENSP00000279146.3:p.Asp166=
ENST00000525341.1:c.149_150delinsAC	ENSP00000476993.1:p.Asp50=
ENST00000528641.6:c.308_309delinsAC	ENSP00000434982.2:p.Asp103=
NM_001302959.1:c.320_321delinsAC	NP_001289888.1:p.Asp107=
NM_001302960.1:c.497_498delinsAC	NP_001289889.1:p.Asp166=
NM_003977.3:c.497_498delinsAC	NP_003968.3:p.Asp166=
XM_024448761.1:c.497_498delinsAC	XP_024304529.1:p.Asp166=
NM_003977.4:c.497_498delinsAC MANE Select	NP_003968.3:p.Asp166=
NM_001302960.2:c.497_498delinsAC	NP_001289889.1:p.Asp166=
NM_001302959.2:c.320_321delinsAC	NP_001289888.1:p.Asp107=