Canonical Allele Identifier: CA2507801261
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490135_67490136insTC , CM000673.2:g.67490135_67490136insTC GRCh38
NC_000011.9:g.67257606_67257607insTC , CM000673.1:g.67257606_67257607insTC GRCh37
NC_000011.8:g.67014182_67014183insTC NCBI36
NG_008969.1:g.12102_12103insTC , LRG_460:g.12102_12103insTC

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.543_544insTC
ENST00000528641.7:c.377_378insTC ENSP00000434982.3:p.Leu126PhefsTer8
ENST00000529797.2:n.1078_1079insTC
ENST00000682324.1:c.468+680_468+681insTC ENSP00000508017.1:n.468+680_468+681insTC
ENST00000682659.1:c.197_198insTC ENSP00000507351.1:p.Leu66PhefsTer8
ENST00000682699.1:c.566_567insTC ENSP00000507935.1:p.Leu189PhefsTer8
ENST00000683237.1:c.566_567insTC ENSP00000507343.1:p.Leu189PhefsTer8
ENST00000683856.1:c.389_390insTC ENSP00000507979.1:p.Leu130PhefsTer8
ENST00000684006.1:c.566_567insTC ENSP00000507269.1:p.Leu189PhefsTer8
ENST00000684657.1:c.386_387insTC ENSP00000507961.1:p.Leu129PhefsTer8
ENST00000279146.8:c.566_567insTC MANE Select ENSP00000279146.3:p.Leu189PhefsTer8
ENST00000279146.7:c.566_567insTC ENSP00000279146.3:p.Leu189PhefsTer8
ENST00000525341.1:c.218_219insTC ENSP00000476993.1:p.Leu73PhefsTer8
ENST00000528641.6:c.377_378insTC ENSP00000434982.2:p.Leu126PhefsTer8
NM_001302959.1:c.389_390insTC NP_001289888.1:p.Leu130PhefsTer8
NM_001302960.1:c.566_567insTC NP_001289889.1:p.Leu189PhefsTer8
NM_003977.3:c.566_567insTC NP_003968.3:p.Leu189PhefsTer8
XM_024448761.1:c.566_567insTC XP_024304529.1:p.Leu189PhefsTer8
NM_003977.4:c.566_567insTC MANE Select NP_003968.3:p.Leu189PhefsTer8
NM_001302960.2:c.566_567insTC NP_001289889.1:p.Leu189PhefsTer8
NM_001302959.2:c.389_390insTC NP_001289888.1:p.Leu130PhefsTer8