Canonical Allele Identifier: CA2624266221
Gene: AP1G2 HGNC NCBI
AP1G2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23563864_23563867del , CM000676.2:g.23563864_23563867del GRCh38
NC_000014.8:g.24033073_24033076del , CM000676.1:g.24033073_24033076del GRCh37
NC_000014.7:g.23102913_23102916del NCBI36
NG_011937.1:g.9204_9207del

Transcript Alleles

HGVS Amino-acid change
ENST00000397120.8:c.1092-11_1092-8del (AP1G2) MANE Select ENSP00000380309.3:n.1092-11_1092-8del
ENST00000308724.9:c.1092-11_1092-8del (AP1G2) ENSP00000312442.5:n.1092-11_1092-8del
ENST00000397120.7:c.1092-11_1092-8del (AP1G2) ENSP00000380309.3:n.1092-11_1092-8del
ENST00000460049.6:n.1265-11_1265-8del (AP1G2)
ENST00000465445.6:n.1140_1143del (AP1G2)
ENST00000535852.6:n.1032-11_1032-8del (AP1G2)
ENST00000554554.5:n.83_86del (AP1G2)
ENST00000554977.1:n.409-11_409-8del (AP1G2)
ENST00000555789.5:n.41-11_41-8del (AP1G2)
ENST00000555974.1:n.47-11_47-8del (AP1G2)
ENST00000556741.5:n.51-11_51-8del (AP1G2)
ENST00000557162.1:c.241-11_241-8del (AP1G2)
NM_001282474.1:c.-52-11_-52-8del (AP1G2) NP_001269403.1:n.-52-11_-52-8del
NM_001282475.1:c.876-11_876-8del (AP1G2) NP_001269404.1:n.876-11_876-8del
NM_003917.4:c.1092-11_1092-8del (AP1G2) NP_003908.1:n.1092-11_1092-8del
NR_110555.1:n.778-863_778-860del (AP1G2-AS1)
XM_005268167.2:c.1263-11_1263-8del (AP1G2) XP_005268224.1:n.1263-11_1263-8del
XM_005268168.3:c.1263-11_1263-8del (AP1G2) XP_005268225.1:n.1263-11_1263-8del
XM_005268169.2:c.1263-11_1263-8del (AP1G2) XP_005268226.1:n.1263-11_1263-8del
XM_005268170.2:c.1263-11_1263-8del (AP1G2) XP_005268227.1:n.1263-11_1263-8del
XM_005268172.2:c.1092-11_1092-8del (AP1G2) XP_005268229.1:n.1092-11_1092-8del
XM_005268173.2:c.1092-11_1092-8del (AP1G2) XP_005268230.1:n.1092-11_1092-8del
XM_005268174.2:c.876-11_876-8del (AP1G2) XP_005268231.1:n.876-11_876-8del
XM_005268175.2:c.876-11_876-8del (AP1G2) XP_005268232.1:n.876-11_876-8del
XM_005268177.2:c.705-11_705-8del (AP1G2) XP_005268234.1:n.705-11_705-8del
XM_005268178.2:c.705-11_705-8del (AP1G2) XP_005268235.1:n.705-11_705-8del
XM_005268179.2:c.705-11_705-8del (AP1G2) XP_005268236.1:n.705-11_705-8del
XM_005268180.3:c.657-11_657-8del (AP1G2) XP_005268237.1:n.657-11_657-8del
XM_005268181.2:c.1365-11_1365-8del (AP1G2) XP_005268238.1:n.1365-11_1365-8del
XM_005268182.2:c.462-11_462-8del (AP1G2) XP_005268239.1:n.462-11_462-8del
XM_006720301.2:c.1263-11_1263-8del (AP1G2) XP_006720364.1:n.1263-11_1263-8del
XM_011537282.1:c.1263-11_1263-8del (AP1G2) XP_011535584.1:n.1263-11_1263-8del
XM_011537283.1:c.1263-11_1263-8del (AP1G2) XP_011535585.1:n.1263-11_1263-8del
XM_011537284.1:c.1365-11_1365-8del (AP1G2) XP_011535586.1:n.1365-11_1365-8del
XM_011537285.1:c.1365-11_1365-8del (AP1G2) XP_011535587.1:n.1365-11_1365-8del
XM_011537286.1:c.-63_-60del (AP1G2) XP_011535588.1:n.-63_-60del
XR_943550.1:n.1264-11_1264-8del (AP1G2)
XR_943551.1:n.1404-11_1404-8del (AP1G2)
XR_943552.1:n.1404-11_1404-8del (AP1G2)
XR_943553.1:n.1264-11_1264-8del (AP1G2)
XR_943554.1:n.1504_1507del (AP1G2)
XR_943555.1:n.1326-11_1326-8del (AP1G2)
NM_001354673.1:c.705-11_705-8del (AP1G2) NP_001341602.1:n.705-11_705-8del
NM_001354674.1:c.-52-11_-52-8del (AP1G2) NP_001341603.1:n.-52-11_-52-8del
NM_001354675.1:c.-63_-60del (AP1G2) NP_001341604.1:n.-63_-60del
NM_001354677.1:c.-63_-60del (AP1G2) NP_001341606.1:n.-63_-60del
NM_001354681.1:c.-52-11_-52-8del (AP1G2) NP_001341610.1:n.-52-11_-52-8del
NR_148937.1:n.1509_1512del (AP1G2)
NR_148938.1:n.1310_1313del (AP1G2)
XM_005268167.3:c.1263-11_1263-8del (AP1G2) XP_005268224.1:n.1263-11_1263-8del
XM_005268168.5:c.1263-11_1263-8del (AP1G2) XP_005268225.1:n.1263-11_1263-8del
XM_005268169.3:c.1263-11_1263-8del (AP1G2) XP_005268226.1:n.1263-11_1263-8del
XM_005268170.3:c.1263-11_1263-8del (AP1G2) XP_005268227.1:n.1263-11_1263-8del
XM_005268172.3:c.1092-11_1092-8del (AP1G2) XP_005268229.1:n.1092-11_1092-8del
XM_005268173.3:c.1092-11_1092-8del (AP1G2) XP_005268230.1:n.1092-11_1092-8del
XM_005268174.3:c.876-11_876-8del (AP1G2) XP_005268231.1:n.876-11_876-8del
XM_005268175.3:c.876-11_876-8del (AP1G2) XP_005268232.1:n.876-11_876-8del
XM_005268178.4:c.705-11_705-8del (AP1G2) XP_005268235.1:n.705-11_705-8del
XM_005268179.3:c.705-11_705-8del (AP1G2) XP_005268236.1:n.705-11_705-8del
XM_005268180.4:c.657-11_657-8del (AP1G2) XP_005268237.1:n.657-11_657-8del
XM_005268182.3:c.462-11_462-8del (AP1G2) XP_005268239.1:n.462-11_462-8del
XM_006720301.3:c.1263-11_1263-8del (AP1G2) XP_006720364.1:n.1263-11_1263-8del
XM_011537283.3:c.1263-11_1263-8del (AP1G2) XP_011535585.1:n.1263-11_1263-8del
XM_017021740.1:c.1263-11_1263-8del (AP1G2) XP_016877229.1:n.1263-11_1263-8del
XM_017021741.1:c.1122-11_1122-8del (AP1G2) XP_016877230.1:n.1122-11_1122-8del
XM_017021742.2:c.876-11_876-8del (AP1G2) XP_016877231.1:n.876-11_876-8del
XM_017021745.1:c.1092-11_1092-8del (AP1G2) XP_016877234.1:n.1092-11_1092-8del
XM_024449738.1:c.-63_-60del (AP1G2) XP_024305506.1:n.-63_-60del
XR_001750583.2:n.1264-11_1264-8del (AP1G2)
XR_001750584.2:n.1264-11_1264-8del (AP1G2)
XR_001750586.1:n.1264-11_1264-8del (AP1G2)
XR_001750587.1:n.1264-11_1264-8del (AP1G2)
XR_001750588.2:n.1717-11_1717-8del (AP1G2)
XR_001750589.1:n.1504_1507del (AP1G2)
XR_001750590.2:n.1326-11_1326-8del (AP1G2)
XR_002957567.1:n.1264-11_1264-8del (AP1G2)
XR_002957568.1:n.1233-11_1233-8del (AP1G2)
XR_002957569.1:n.1147-11_1147-8del (AP1G2)
XR_002957570.1:n.1504_1507del (AP1G2)
NM_001282474.2:c.-52-11_-52-8del (AP1G2) NP_001269403.1:n.-52-11_-52-8del
NM_001282475.2:c.876-11_876-8del (AP1G2) NP_001269404.1:n.876-11_876-8del
NM_001354673.2:c.705-11_705-8del (AP1G2) NP_001341602.1:n.705-11_705-8del
NM_001354674.2:c.-52-11_-52-8del (AP1G2) NP_001341603.1:n.-52-11_-52-8del
NM_001354675.2:c.-63_-60del (AP1G2) NP_001341604.1:n.-63_-60del
NM_001354677.2:c.-63_-60del (AP1G2) NP_001341606.1:n.-63_-60del
NM_001354681.2:c.-52-11_-52-8del (AP1G2) NP_001341610.1:n.-52-11_-52-8del
NM_003917.5:c.1092-11_1092-8del (AP1G2) MANE Select NP_003908.1:n.1092-11_1092-8del
NR_148937.2:n.1787_1790del (AP1G2)
NR_148938.2:n.1313_1316del (AP1G2)