Canonical Allele Identifier: CA2630857389

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.724038_724039insGC , CM000678.2:g.724038_724039insGC GRCh38
NC_000016.9:g.774038_774039insGC , CM000678.1:g.774038_774039insGC GRCh37
NC_000016.8:g.714039_714040insGC NCBI36
NG_032932.1:g.7435_7436insGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000682391.1:n.1596+67_1596+68insGC (CCDC78)
ENST00000345165.10:c.1053+67_1053+68insGC (CCDC78) MANE Select ENSP00000316851.5:n.1053+67_1053+68insGC
ENST00000293889.10:c.1053+67_1053+68insGC (CCDC78) ENSP00000293889.6:n.1053+67_1053+68insGC
ENST00000345165.8:c.599+67_599+68insGC (CCDC78)
ENST00000463539.5:n.1375+67_1375+68insGC (CCDC78)
ENST00000466708.5:n.1397+67_1397+68insGC (CCDC78)
ENST00000478979.5:n.1598_1599insGC (CCDC78)
ENST00000481804.5:n.2031+67_2031+68insGC (CCDC78)
ENST00000482152.1:n.414+67_414+68insGC (CCDC78)
ENST00000482878.5:n.2001_2002insGC (CCDC78)
ENST00000485091.5:n.1206+67_1206+68insGC (CCDC78)
ENST00000620831.4:c.-49-38594_-49-38593insGC (MSLN) ENSP00000482893.1:n.-49-38594_-49-38593insGC
NM_001031737.2:c.1053+67_1053+68insGC (CCDC78) NP_001026907.2:n.1053+67_1053+68insGC
XM_006720838.1:c.1275+67_1275+68insGC (CCDC78) XP_006720901.1:n.1275+67_1275+68insGC
XM_006720843.2:c.1053+67_1053+68insGC (CCDC78) XP_006720906.1:n.1053+67_1053+68insGC
XM_011522356.1:c.1500+67_1500+68insGC (CCDC78) XP_011520658.1:n.1500+67_1500+68insGC
XM_011522357.1:c.1488+67_1488+68insGC (CCDC78) XP_011520659.1:n.1488+67_1488+68insGC
XM_011522358.1:c.1500+67_1500+68insGC (CCDC78) XP_011520660.1:n.1500+67_1500+68insGC
XM_011522359.1:c.1467+67_1467+68insGC (CCDC78) XP_011520661.1:n.1467+67_1467+68insGC
XM_011522360.1:c.1455+67_1455+68insGC (CCDC78) XP_011520662.1:n.1455+67_1455+68insGC
XM_011522361.1:c.1500+67_1500+68insGC (CCDC78) XP_011520663.1:n.1500+67_1500+68insGC
XM_011522362.1:c.1500+67_1500+68insGC (CCDC78) XP_011520664.1:n.1500+67_1500+68insGC
XM_011522363.1:c.1500+67_1500+68insGC (CCDC78) XP_011520665.1:n.1500+67_1500+68insGC
XM_011522364.1:c.1500+67_1500+68insGC (CCDC78) XP_011520666.1:n.1500+67_1500+68insGC
XM_011522365.1:c.1287+67_1287+68insGC (CCDC78) XP_011520667.1:n.1287+67_1287+68insGC
XM_011522366.1:c.1278+67_1278+68insGC (CCDC78) XP_011520668.1:n.1278+67_1278+68insGC
XM_011522367.1:c.1119+67_1119+68insGC (CCDC78) XP_011520669.1:n.1119+67_1119+68insGC
XM_011522368.1:c.1107+67_1107+68insGC (CCDC78) XP_011520670.1:n.1107+67_1107+68insGC
XM_011522369.1:c.1065+67_1065+68insGC (CCDC78) XP_011520671.1:n.1065+67_1065+68insGC
XM_011522370.1:c.897+67_897+68insGC (CCDC78) XP_011520672.1:n.897+67_897+68insGC
XM_011522371.1:c.612+67_612+68insGC (CCDC78) XP_011520673.1:n.612+67_612+68insGC
XM_006720843.4:c.1053+67_1053+68insGC (CCDC78) XP_006720906.1:n.1053+67_1053+68insGC
XM_011522358.2:c.1500+67_1500+68insGC (CCDC78) XP_011520660.1:n.1500+67_1500+68insGC
XM_011522371.2:c.612+67_612+68insGC (CCDC78) XP_011520673.1:n.612+67_612+68insGC
XM_017022929.1:c.1500+67_1500+68insGC (CCDC78) XP_016878418.1:n.1500+67_1500+68insGC
XM_017022930.1:c.600+67_600+68insGC (CCDC78) XP_016878419.1:n.600+67_600+68insGC
XM_017022931.1:c.-303_-302insGC (CCDC78) XP_016878420.1:n.-303_-302insGC
XM_024450150.1:c.330+67_330+68insGC (CCDC78) XP_024305918.1:n.330+67_330+68insGC
XR_001751835.1:n.1839+67_1839+68insGC (CCDC78)
XR_001751836.1:n.1818+67_1818+68insGC (CCDC78)
XR_001751837.1:n.1596+67_1596+68insGC (CCDC78)
XR_001751838.1:n.1942+67_1942+68insGC (CCDC78)
XR_001751839.1:n.1404+67_1404+68insGC (CCDC78)
NM_001031737.3:c.1053+67_1053+68insGC (CCDC78) NP_001026907.2:n.1053+67_1053+68insGC
NM_001378030.1:c.1053+67_1053+68insGC (CCDC78) MANE Select NP_001364959.1:n.1053+67_1053+68insGC
NM_001378031.1:c.953+283_953+284insGC (CCDC78) NP_001364960.1:n.953+283_953+284insGC
NM_001378033.1:c.486+67_486+68insGC (CCDC78) NP_001364962.1:n.486+67_486+68insGC
NR_165382.1:n.1610+67_1610+68insGC (CCDC78)
NR_165383.1:n.1256+67_1256+68insGC (CCDC78)
NR_165384.1:n.1221+67_1221+68insGC (CCDC78)
NR_165385.1:n.1321+67_1321+68insGC (CCDC78)
NR_165386.1:n.1388+67_1388+68insGC (CCDC78)