Canonical Allele Identifier: CA2630857181

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-724015-TTGAGCCCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724016_724023del , CM000678.2:g.724016_724023del	GRCh38
NC_000016.9:g.774016_774023del , CM000678.1:g.774016_774023del	GRCh37
NC_000016.8:g.714017_714024del	NCBI36
NG_032932.1:g.7451_7458del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1596+83_1597-80del (CCDC78)
ENST00000345165.10:c.1053+83_1054-80del (CCDC78) MANE Select	ENSP00000316851.5:n.1053+83_1054-80del
ENST00000293889.10:c.1053+83_1054-80del (CCDC78)	ENSP00000293889.6:n.1053+83_1054-80del
ENST00000345165.8:c.599+83_600-80del (CCDC78)
ENST00000463539.5:n.1375+83_1376-80del (CCDC78)
ENST00000466708.5:n.1397+83_1398-80del (CCDC78)
ENST00000478979.5:n.1614_1621del (CCDC78)
ENST00000481804.5:n.2031+83_2032-80del (CCDC78)
ENST00000482152.1:n.414+83_415-80del (CCDC78)
ENST00000482878.5:n.2017_2024del (CCDC78)
ENST00000485091.5:n.1206+83_1207-80del (CCDC78)
ENST00000620831.4:c.-49-38616_-49-38609del (MSLN)	ENSP00000482893.1:n.-49-38616_-49-38609del
NM_001031737.2:c.1053+83_1054-80del (CCDC78)	NP_001026907.2:n.1053+83_1054-80del
XM_006720838.1:c.1275+83_1276-80del (CCDC78)	XP_006720901.1:n.1275+83_1276-80del
XM_006720843.2:c.1053+83_1054-80del (CCDC78)	XP_006720906.1:n.1053+83_1054-80del
XM_011522356.1:c.1500+83_1501-80del (CCDC78)	XP_011520658.1:n.1500+83_1501-80del
XM_011522357.1:c.1488+83_1489-80del (CCDC78)	XP_011520659.1:n.1488+83_1489-80del
XM_011522358.1:c.1500+83_1501-80del (CCDC78)	XP_011520660.1:n.1500+83_1501-80del
XM_011522359.1:c.1467+83_1468-80del (CCDC78)	XP_011520661.1:n.1467+83_1468-80del
XM_011522360.1:c.1455+83_1456-80del (CCDC78)	XP_011520662.1:n.1455+83_1456-80del
XM_011522361.1:c.1500+83_1501-80del (CCDC78)	XP_011520663.1:n.1500+83_1501-80del
XM_011522362.1:c.1500+83_1501-80del (CCDC78)	XP_011520664.1:n.1500+83_1501-80del
XM_011522363.1:c.1500+83_1501-80del (CCDC78)	XP_011520665.1:n.1500+83_1501-80del
XM_011522364.1:c.1500+83_1501-80del (CCDC78)	XP_011520666.1:n.1500+83_1501-80del
XM_011522365.1:c.1287+83_1288-80del (CCDC78)	XP_011520667.1:n.1287+83_1288-80del
XM_011522366.1:c.1278+83_1279-80del (CCDC78)	XP_011520668.1:n.1278+83_1279-80del
XM_011522367.1:c.1119+83_1120-80del (CCDC78)	XP_011520669.1:n.1119+83_1120-80del
XM_011522368.1:c.1107+83_1108-80del (CCDC78)	XP_011520670.1:n.1107+83_1108-80del
XM_011522369.1:c.1065+83_1066-80del (CCDC78)	XP_011520671.1:n.1065+83_1066-80del
XM_011522370.1:c.897+83_898-80del (CCDC78)	XP_011520672.1:n.897+83_898-80del
XM_011522371.1:c.612+83_613-80del (CCDC78)	XP_011520673.1:n.612+83_613-80del
XM_006720843.4:c.1053+83_1054-80del (CCDC78)	XP_006720906.1:n.1053+83_1054-80del
XM_011522358.2:c.1500+83_1501-80del (CCDC78)	XP_011520660.1:n.1500+83_1501-80del
XM_011522371.2:c.612+83_613-80del (CCDC78)	XP_011520673.1:n.612+83_613-80del
XM_017022929.1:c.1500+83_1501-80del (CCDC78)	XP_016878418.1:n.1500+83_1501-80del
XM_017022930.1:c.600+83_601-80del (CCDC78)	XP_016878419.1:n.600+83_601-80del
XM_017022931.1:c.-287_-280del (CCDC78)	XP_016878420.1:n.-287_-280del
XM_024450150.1:c.330+83_331-80del (CCDC78)	XP_024305918.1:n.330+83_331-80del
XR_001751835.1:n.1839+83_1840-80del (CCDC78)
XR_001751836.1:n.1818+83_1819-80del (CCDC78)
XR_001751837.1:n.1596+83_1597-80del (CCDC78)
XR_001751838.1:n.1942+83_1943-80del (CCDC78)
XR_001751839.1:n.1404+83_1405-80del (CCDC78)
NM_001031737.3:c.1053+83_1054-80del (CCDC78)	NP_001026907.2:n.1053+83_1054-80del
NM_001378030.1:c.1053+83_1054-80del (CCDC78) MANE Select	NP_001364959.1:n.1053+83_1054-80del
NM_001378031.1:c.953+299_953+306del (CCDC78)	NP_001364960.1:n.953+299_953+306del
NM_001378033.1:c.486+83_487-80del (CCDC78)	NP_001364962.1:n.486+83_487-80del
NR_165382.1:n.1610+83_1611-80del (CCDC78)
NR_165383.1:n.1256+83_1257-80del (CCDC78)
NR_165384.1:n.1221+83_1222-80del (CCDC78)
NR_165385.1:n.1321+83_1322-80del (CCDC78)
NR_165386.1:n.1388+83_1389-80del (CCDC78)