Canonical Allele Identifier: CA2731817173

Linked Data

dbSNP Id: rs2151549506

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.723998del , CM000678.2:g.723998del GRCh38
NC_000016.9:g.773998del , CM000678.1:g.773998del GRCh37
NC_000016.8:g.713999del NCBI36
NG_032932.1:g.7478del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682391.1:n.1597-60del (CCDC78)
ENST00000345165.10:c.1054-60del (CCDC78) MANE Select ENSP00000316851.5:n.1054-60del
ENST00000293889.10:c.1054-60del (CCDC78) ENSP00000293889.6:n.1054-60del
ENST00000345165.8:c.600-60del (CCDC78)
ENST00000463539.5:n.1376-60del (CCDC78)
ENST00000466708.5:n.1398-60del (CCDC78)
ENST00000478979.5:n.1641del (CCDC78)
ENST00000481804.5:n.2032-60del (CCDC78)
ENST00000482152.1:n.415-60del (CCDC78)
ENST00000482878.5:n.2044del (CCDC78)
ENST00000485091.5:n.1207-60del (CCDC78)
ENST00000620831.4:c.-49-38634del (MSLN) ENSP00000482893.1:n.-49-38634del
NM_001031737.2:c.1054-60del (CCDC78) NP_001026907.2:n.1054-60del
XM_006720838.1:c.1276-60del (CCDC78) XP_006720901.1:n.1276-60del
XM_006720843.2:c.1054-60del (CCDC78) XP_006720906.1:n.1054-60del
XM_011522356.1:c.1501-60del (CCDC78) XP_011520658.1:n.1501-60del
XM_011522357.1:c.1489-60del (CCDC78) XP_011520659.1:n.1489-60del
XM_011522358.1:c.1501-60del (CCDC78) XP_011520660.1:n.1501-60del
XM_011522359.1:c.1468-60del (CCDC78) XP_011520661.1:n.1468-60del
XM_011522360.1:c.1456-60del (CCDC78) XP_011520662.1:n.1456-60del
XM_011522361.1:c.1501-60del (CCDC78) XP_011520663.1:n.1501-60del
XM_011522362.1:c.1501-60del (CCDC78) XP_011520664.1:n.1501-60del
XM_011522363.1:c.1501-60del (CCDC78) XP_011520665.1:n.1501-60del
XM_011522364.1:c.1501-60del (CCDC78) XP_011520666.1:n.1501-60del
XM_011522365.1:c.1288-60del (CCDC78) XP_011520667.1:n.1288-60del
XM_011522366.1:c.1279-60del (CCDC78) XP_011520668.1:n.1279-60del
XM_011522367.1:c.1120-60del (CCDC78) XP_011520669.1:n.1120-60del
XM_011522368.1:c.1108-60del (CCDC78) XP_011520670.1:n.1108-60del
XM_011522369.1:c.1066-60del (CCDC78) XP_011520671.1:n.1066-60del
XM_011522370.1:c.898-60del (CCDC78) XP_011520672.1:n.898-60del
XM_011522371.1:c.613-60del (CCDC78) XP_011520673.1:n.613-60del
XM_006720843.4:c.1054-60del (CCDC78) XP_006720906.1:n.1054-60del
XM_011522358.2:c.1501-60del (CCDC78) XP_011520660.1:n.1501-60del
XM_011522371.2:c.613-60del (CCDC78) XP_011520673.1:n.613-60del
XM_017022929.1:c.1501-60del (CCDC78) XP_016878418.1:n.1501-60del
XM_017022930.1:c.601-60del (CCDC78) XP_016878419.1:n.601-60del
XM_017022931.1:c.-260del (CCDC78) XP_016878420.1:n.-260del
XM_024450150.1:c.331-60del (CCDC78) XP_024305918.1:n.331-60del
XR_001751835.1:n.1840-60del (CCDC78)
XR_001751836.1:n.1819-60del (CCDC78)
XR_001751837.1:n.1597-60del (CCDC78)
XR_001751838.1:n.1943-60del (CCDC78)
XR_001751839.1:n.1405-60del (CCDC78)
NM_001031737.3:c.1054-60del (CCDC78) NP_001026907.2:n.1054-60del
NM_001378030.1:c.1054-60del (CCDC78) MANE Select NP_001364959.1:n.1054-60del
NM_001378031.1:c.953+326del (CCDC78) NP_001364960.1:n.953+326del
NM_001378033.1:c.487-60del (CCDC78) NP_001364962.1:n.487-60del
NR_165382.1:n.1611-60del (CCDC78)
NR_165383.1:n.1257-60del (CCDC78)
NR_165384.1:n.1222-60del (CCDC78)
NR_165385.1:n.1322-60del (CCDC78)
NR_165386.1:n.1389-60del (CCDC78)