Canonical Allele Identifier: CA2630857722

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-724049-GCAGTGGGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724050_724057del , CM000678.2:g.724050_724057del	GRCh38
NC_000016.9:g.774050_774057del , CM000678.1:g.774050_774057del	GRCh37
NC_000016.8:g.714051_714058del	NCBI36
NG_032932.1:g.7417_7424del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1596+49_1596+56del (CCDC78)
ENST00000345165.10:c.1053+49_1053+56del (CCDC78) MANE Select	ENSP00000316851.5:n.1053+49_1053+56del
ENST00000293889.10:c.1053+49_1053+56del (CCDC78)	ENSP00000293889.6:n.1053+49_1053+56del
ENST00000345165.8:c.599+49_599+56del (CCDC78)
ENST00000463539.5:n.1375+49_1375+56del (CCDC78)
ENST00000466708.5:n.1397+49_1397+56del (CCDC78)
ENST00000478979.5:n.1580_1587del (CCDC78)
ENST00000481804.5:n.2031+49_2031+56del (CCDC78)
ENST00000482152.1:n.414+49_414+56del (CCDC78)
ENST00000482878.5:n.1983_1990del (CCDC78)
ENST00000485091.5:n.1206+49_1206+56del (CCDC78)
ENST00000620831.4:c.-49-38582_-49-38575del (MSLN)	ENSP00000482893.1:n.-49-38582_-49-38575del
NM_001031737.2:c.1053+49_1053+56del (CCDC78)	NP_001026907.2:n.1053+49_1053+56del
XM_006720838.1:c.1275+49_1275+56del (CCDC78)	XP_006720901.1:n.1275+49_1275+56del
XM_006720843.2:c.1053+49_1053+56del (CCDC78)	XP_006720906.1:n.1053+49_1053+56del
XM_011522356.1:c.1500+49_1500+56del (CCDC78)	XP_011520658.1:n.1500+49_1500+56del
XM_011522357.1:c.1488+49_1488+56del (CCDC78)	XP_011520659.1:n.1488+49_1488+56del
XM_011522358.1:c.1500+49_1500+56del (CCDC78)	XP_011520660.1:n.1500+49_1500+56del
XM_011522359.1:c.1467+49_1467+56del (CCDC78)	XP_011520661.1:n.1467+49_1467+56del
XM_011522360.1:c.1455+49_1455+56del (CCDC78)	XP_011520662.1:n.1455+49_1455+56del
XM_011522361.1:c.1500+49_1500+56del (CCDC78)	XP_011520663.1:n.1500+49_1500+56del
XM_011522362.1:c.1500+49_1500+56del (CCDC78)	XP_011520664.1:n.1500+49_1500+56del
XM_011522363.1:c.1500+49_1500+56del (CCDC78)	XP_011520665.1:n.1500+49_1500+56del
XM_011522364.1:c.1500+49_1500+56del (CCDC78)	XP_011520666.1:n.1500+49_1500+56del
XM_011522365.1:c.1287+49_1287+56del (CCDC78)	XP_011520667.1:n.1287+49_1287+56del
XM_011522366.1:c.1278+49_1278+56del (CCDC78)	XP_011520668.1:n.1278+49_1278+56del
XM_011522367.1:c.1119+49_1119+56del (CCDC78)	XP_011520669.1:n.1119+49_1119+56del
XM_011522368.1:c.1107+49_1107+56del (CCDC78)	XP_011520670.1:n.1107+49_1107+56del
XM_011522369.1:c.1065+49_1065+56del (CCDC78)	XP_011520671.1:n.1065+49_1065+56del
XM_011522370.1:c.897+49_897+56del (CCDC78)	XP_011520672.1:n.897+49_897+56del
XM_011522371.1:c.612+49_612+56del (CCDC78)	XP_011520673.1:n.612+49_612+56del
XM_006720843.4:c.1053+49_1053+56del (CCDC78)	XP_006720906.1:n.1053+49_1053+56del
XM_011522358.2:c.1500+49_1500+56del (CCDC78)	XP_011520660.1:n.1500+49_1500+56del
XM_011522371.2:c.612+49_612+56del (CCDC78)	XP_011520673.1:n.612+49_612+56del
XM_017022929.1:c.1500+49_1500+56del (CCDC78)	XP_016878418.1:n.1500+49_1500+56del
XM_017022930.1:c.600+49_600+56del (CCDC78)	XP_016878419.1:n.600+49_600+56del
XM_017022931.1:c.-321_-314del (CCDC78)	XP_016878420.1:n.-321_-314del
XM_024450150.1:c.330+49_330+56del (CCDC78)	XP_024305918.1:n.330+49_330+56del
XR_001751835.1:n.1839+49_1839+56del (CCDC78)
XR_001751836.1:n.1818+49_1818+56del (CCDC78)
XR_001751837.1:n.1596+49_1596+56del (CCDC78)
XR_001751838.1:n.1942+49_1942+56del (CCDC78)
XR_001751839.1:n.1404+49_1404+56del (CCDC78)
NM_001031737.3:c.1053+49_1053+56del (CCDC78)	NP_001026907.2:n.1053+49_1053+56del
NM_001378030.1:c.1053+49_1053+56del (CCDC78) MANE Select	NP_001364959.1:n.1053+49_1053+56del
NM_001378031.1:c.953+265_953+272del (CCDC78)	NP_001364960.1:n.953+265_953+272del
NM_001378033.1:c.486+49_486+56del (CCDC78)	NP_001364962.1:n.486+49_486+56del
NR_165382.1:n.1610+49_1610+56del (CCDC78)
NR_165383.1:n.1256+49_1256+56del (CCDC78)
NR_165384.1:n.1221+49_1221+56del (CCDC78)
NR_165385.1:n.1321+49_1321+56del (CCDC78)
NR_165386.1:n.1388+49_1388+56del (CCDC78)