Canonical Allele Identifier: CA2695214807

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490811_67490812del , CM000673.2:g.67490811_67490812del	GRCh38
NC_000011.9:g.67258282_67258283del , CM000673.1:g.67258282_67258283del	GRCh37
NC_000011.8:g.67014858_67014859del	NCBI36
NG_008969.1:g.12778_12779del , LRG_460:g.12778_12779del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1118_1119del
ENST00000528641.7:c.622_623del	ENSP00000434982.3:p.Arg208GlyfsTer16
ENST00000529797.2:n.1653_1654del
ENST00000682324.1:c.469-186_469-185del	ENSP00000508017.1:n.469-186_469-185del
ENST00000682659.1:c.442_443del	ENSP00000507351.1:p.Arg148GlyfsTer16
ENST00000682699.1:c.811_812del	ENSP00000507935.1:p.Arg271GlyfsTer16
ENST00000683237.1:c.803_804del	ENSP00000507343.1:p.Ala268GlyfsTer?
ENST00000683856.1:c.634_635del	ENSP00000507979.1:p.Arg212GlyfsTer16
ENST00000684006.1:c.800_801del	ENSP00000507269.1:p.Ala267GlyfsTer?
ENST00000684657.1:c.631_632del	ENSP00000507961.1:p.Arg211GlyfsTer16
ENST00000279146.8:c.811_812del MANE Select	ENSP00000279146.3:p.Arg271GlyfsTer16
ENST00000279146.7:c.811_812del	ENSP00000279146.3:p.Arg271GlyfsTer16
ENST00000528641.6:c.622_623del	ENSP00000434982.2:p.Arg208GlyfsTer16
NM_001302959.1:c.634_635del	NP_001289888.1:p.Arg212GlyfsTer16
NM_001302960.1:c.803_804del	NP_001289889.1:p.Ala268GlyfsTer?
NM_003977.3:c.811_812del	NP_003968.3:p.Arg271GlyfsTer16
XM_024448761.1:c.811_812del	XP_024304529.1:p.Arg271GlyfsTer16
NM_003977.4:c.811_812del MANE Select	NP_003968.3:p.Arg271GlyfsTer16
NM_001302960.2:c.803_804del	NP_001289889.1:p.Ala268GlyfsTer?
NM_001302959.2:c.634_635del	NP_001289888.1:p.Arg212GlyfsTer16