Canonical Allele Identifier: CA2534074633
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490133_67490134insCTGCGGCACCCCCTCGAC , CM000673.2:g.67490133_67490134insCTGCGGCACCCCCTCGAC GRCh38
NC_000011.9:g.67257604_67257605insCTGCGGCACCCCCTCGAC , CM000673.1:g.67257604_67257605insCTGCGGCACCCCCTCGAC GRCh37
NC_000011.8:g.67014180_67014181insCTGCGGCACCCCCTCGAC NCBI36
NG_008969.1:g.12100_12101insCTGCGGCACCCCCTCGAC , LRG_460:g.12100_12101insCTGCGGCACCCCCTCGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000525341.2:c.541_542insCTGCGGCACCCCCTCGAC
ENST00000528641.7:c.375_376insCTGCGGCACCCCCTCGAC ENSP00000434982.3:p.Arg125_Leu126insLeuArgHisProLeuAsp
ENST00000529797.2:n.1076_1077insCTGCGGCACCCCCTCGAC
ENST00000682324.1:c.468+678_468+679insCTGCGGCACCCCCTCGAC ENSP00000508017.1:n.468+678_468+679insCTGCGGCACCCCCTCGAC
ENST00000682659.1:c.195_196insCTGCGGCACCCCCTCGAC ENSP00000507351.1:p.Arg65_Leu66insLeuArgHisProLeuAsp
ENST00000682699.1:c.564_565insCTGCGGCACCCCCTCGAC ENSP00000507935.1:p.Arg188_Leu189insLeuArgHisProLeuAsp
ENST00000683237.1:c.564_565insCTGCGGCACCCCCTCGAC ENSP00000507343.1:p.Arg188_Leu189insLeuArgHisProLeuAsp
ENST00000683856.1:c.387_388insCTGCGGCACCCCCTCGAC ENSP00000507979.1:p.Arg129_Leu130insLeuArgHisProLeuAsp
ENST00000684006.1:c.564_565insCTGCGGCACCCCCTCGAC ENSP00000507269.1:p.Arg188_Leu189insLeuArgHisProLeuAsp
ENST00000684657.1:c.384_385insCTGCGGCACCCCCTCGAC ENSP00000507961.1:p.Arg128_Leu129insLeuArgHisProLeuAsp
ENST00000279146.8:c.564_565insCTGCGGCACCCCCTCGAC MANE Select ENSP00000279146.3:p.Arg188_Leu189insLeuArgHisProLeuAsp
ENST00000279146.7:c.564_565insCTGCGGCACCCCCTCGAC ENSP00000279146.3:p.Arg188_Leu189insLeuArgHisProLeuAsp
ENST00000525341.1:c.216_217insCTGCGGCACCCCCTCGAC ENSP00000476993.1:p.Arg72_Leu73insLeuArgHisProLeuAsp
ENST00000528641.6:c.375_376insCTGCGGCACCCCCTCGAC ENSP00000434982.2:p.Arg125_Leu126insLeuArgHisProLeuAsp
NM_001302959.1:c.387_388insCTGCGGCACCCCCTCGAC NP_001289888.1:p.Arg129_Leu130insLeuArgHisProLeuAsp
NM_001302960.1:c.564_565insCTGCGGCACCCCCTCGAC NP_001289889.1:p.Arg188_Leu189insLeuArgHisProLeuAsp
NM_003977.3:c.564_565insCTGCGGCACCCCCTCGAC NP_003968.3:p.Arg188_Leu189insLeuArgHisProLeuAsp
XM_024448761.1:c.564_565insCTGCGGCACCCCCTCGAC XP_024304529.1:p.Arg188_Leu189insLeuArgHisProLeuAsp
NM_003977.4:c.564_565insCTGCGGCACCCCCTCGAC MANE Select NP_003968.3:p.Arg188_Leu189insLeuArgHisProLeuAsp
NM_001302960.2:c.564_565insCTGCGGCACCCCCTCGAC NP_001289889.1:p.Arg188_Leu189insLeuArgHisProLeuAsp
NM_001302959.2:c.387_388insCTGCGGCACCCCCTCGAC NP_001289888.1:p.Arg129_Leu130insLeuArgHisProLeuAsp