Canonical Allele Identifier: CA2589945772

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.724069_724070insGGGGGGGGGGGGGGGGCA , CM000678.2:g.724069_724070insGGGGGGGGGGGGGGGGCA GRCh38
NC_000016.9:g.774069_774070insGGGGGGGGGGGGGGGGCA , CM000678.1:g.774069_774070insGGGGGGGGGGGGGGGGCA GRCh37
NC_000016.8:g.714070_714071insGGGGGGGGGGGGGGGGCA NCBI36
NG_032932.1:g.7412_7413insCCCCCCCCCCTGCCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000682391.1:n.1596+44_1596+45insCCCCCCCCCCTGCCCCCC (CCDC78)
ENST00000345165.10:c.1053+44_1053+45insCCCCCCCCCCTGCCCCCC (CCDC78) MANE Select ENSP00000316851.5:n.1053+44_1053+45insCCCCCCCCCCTGCCCCCC
ENST00000293889.10:c.1053+44_1053+45insCCCCCCCCCCTGCCCCCC (CCDC78) ENSP00000293889.6:n.1053+44_1053+45insCCCCCCCCCCTGCCCCCC
ENST00000345165.8:c.599+44_599+45insCCCCCCCCCCTGCCCCCC (CCDC78)
ENST00000463539.5:n.1375+44_1375+45insCCCCCCCCCCTGCCCCCC (CCDC78)
ENST00000466708.5:n.1397+44_1397+45insCCCCCCCCCCTGCCCCCC (CCDC78)
ENST00000478979.5:n.1575_1576insCCCCCCCCCCTGCCCCCC (CCDC78)
ENST00000481804.5:n.2031+44_2031+45insCCCCCCCCCCTGCCCCCC (CCDC78)
ENST00000482152.1:n.414+44_414+45insCCCCCCCCCCTGCCCCCC (CCDC78)
ENST00000482878.5:n.1978_1979insCCCCCCCCCCTGCCCCCC (CCDC78)
ENST00000485091.5:n.1206+44_1206+45insCCCCCCCCCCTGCCCCCC (CCDC78)
ENST00000620831.4:c.-49-38563_-49-38562insGGGGGGGGGGGGGGGGCA (MSLN) ENSP00000482893.1:n.-49-38563_-49-38562insGGGGGGGGGGGGGGGGCA
NM_001031737.2:c.1053+44_1053+45insCCCCCCCCCCTGCCCCCC (CCDC78) NP_001026907.2:n.1053+44_1053+45insCCCCCCCCCCTGCCCCCC
XM_006720838.1:c.1275+44_1275+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_006720901.1:n.1275+44_1275+45insCCCCCCCCCCTGCCCCCC
XM_006720843.2:c.1053+44_1053+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_006720906.1:n.1053+44_1053+45insCCCCCCCCCCTGCCCCCC
XM_011522356.1:c.1500+44_1500+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_011520658.1:n.1500+44_1500+45insCCCCCCCCCCTGCCCCCC
XM_011522357.1:c.1488+44_1488+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_011520659.1:n.1488+44_1488+45insCCCCCCCCCCTGCCCCCC
XM_011522358.1:c.1500+44_1500+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_011520660.1:n.1500+44_1500+45insCCCCCCCCCCTGCCCCCC
XM_011522359.1:c.1467+44_1467+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_011520661.1:n.1467+44_1467+45insCCCCCCCCCCTGCCCCCC
XM_011522360.1:c.1455+44_1455+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_011520662.1:n.1455+44_1455+45insCCCCCCCCCCTGCCCCCC
XM_011522361.1:c.1500+44_1500+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_011520663.1:n.1500+44_1500+45insCCCCCCCCCCTGCCCCCC
XM_011522362.1:c.1500+44_1500+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_011520664.1:n.1500+44_1500+45insCCCCCCCCCCTGCCCCCC
XM_011522363.1:c.1500+44_1500+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_011520665.1:n.1500+44_1500+45insCCCCCCCCCCTGCCCCCC
XM_011522364.1:c.1500+44_1500+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_011520666.1:n.1500+44_1500+45insCCCCCCCCCCTGCCCCCC
XM_011522365.1:c.1287+44_1287+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_011520667.1:n.1287+44_1287+45insCCCCCCCCCCTGCCCCCC
XM_011522366.1:c.1278+44_1278+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_011520668.1:n.1278+44_1278+45insCCCCCCCCCCTGCCCCCC
XM_011522367.1:c.1119+44_1119+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_011520669.1:n.1119+44_1119+45insCCCCCCCCCCTGCCCCCC
XM_011522368.1:c.1107+44_1107+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_011520670.1:n.1107+44_1107+45insCCCCCCCCCCTGCCCCCC
XM_011522369.1:c.1065+44_1065+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_011520671.1:n.1065+44_1065+45insCCCCCCCCCCTGCCCCCC
XM_011522370.1:c.897+44_897+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_011520672.1:n.897+44_897+45insCCCCCCCCCCTGCCCCCC
XM_011522371.1:c.612+44_612+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_011520673.1:n.612+44_612+45insCCCCCCCCCCTGCCCCCC
XM_006720843.4:c.1053+44_1053+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_006720906.1:n.1053+44_1053+45insCCCCCCCCCCTGCCCCCC
XM_011522358.2:c.1500+44_1500+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_011520660.1:n.1500+44_1500+45insCCCCCCCCCCTGCCCCCC
XM_011522371.2:c.612+44_612+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_011520673.1:n.612+44_612+45insCCCCCCCCCCTGCCCCCC
XM_017022929.1:c.1500+44_1500+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_016878418.1:n.1500+44_1500+45insCCCCCCCCCCTGCCCCCC
XM_017022930.1:c.600+44_600+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_016878419.1:n.600+44_600+45insCCCCCCCCCCTGCCCCCC
XM_017022931.1:c.-326_-325insCCCCCCCCCCTGCCCCCC (CCDC78) XP_016878420.1:n.-326_-325insCCCCCCCCCCTGCCCCCC
XM_024450150.1:c.330+44_330+45insCCCCCCCCCCTGCCCCCC (CCDC78) XP_024305918.1:n.330+44_330+45insCCCCCCCCCCTGCCCCCC
XR_001751835.1:n.1839+44_1839+45insCCCCCCCCCCTGCCCCCC (CCDC78)
XR_001751836.1:n.1818+44_1818+45insCCCCCCCCCCTGCCCCCC (CCDC78)
XR_001751837.1:n.1596+44_1596+45insCCCCCCCCCCTGCCCCCC (CCDC78)
XR_001751838.1:n.1942+44_1942+45insCCCCCCCCCCTGCCCCCC (CCDC78)
XR_001751839.1:n.1404+44_1404+45insCCCCCCCCCCTGCCCCCC (CCDC78)
NM_001031737.3:c.1053+44_1053+45insCCCCCCCCCCTGCCCCCC (CCDC78) NP_001026907.2:n.1053+44_1053+45insCCCCCCCCCCTGCCCCCC
NM_001378030.1:c.1053+44_1053+45insCCCCCCCCCCTGCCCCCC (CCDC78) MANE Select NP_001364959.1:n.1053+44_1053+45insCCCCCCCCCCTGCCCCCC
NM_001378031.1:c.953+260_953+261insCCCCCCCCCCTGCCCCCC (CCDC78) NP_001364960.1:n.953+260_953+261insCCCCCCCCCCTGCCCCCC
NM_001378033.1:c.486+44_486+45insCCCCCCCCCCTGCCCCCC (CCDC78) NP_001364962.1:n.486+44_486+45insCCCCCCCCCCTGCCCCCC
NR_165382.1:n.1610+44_1610+45insCCCCCCCCCCTGCCCCCC (CCDC78)
NR_165383.1:n.1256+44_1256+45insCCCCCCCCCCTGCCCCCC (CCDC78)
NR_165384.1:n.1221+44_1221+45insCCCCCCCCCCTGCCCCCC (CCDC78)
NR_165385.1:n.1321+44_1321+45insCCCCCCCCCCTGCCCCCC (CCDC78)
NR_165386.1:n.1388+44_1388+45insCCCCCCCCCCTGCCCCCC (CCDC78)