Canonical Allele Identifier: CA2630857586

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-724045-T-TGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724046_724049dup , CM000678.2:g.724046_724049dup	GRCh38
NC_000016.9:g.774046_774049dup , CM000678.1:g.774046_774049dup	GRCh37
NC_000016.8:g.714047_714050dup	NCBI36
NG_032932.1:g.7425_7428dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1596+57_1596+60dup (CCDC78)
ENST00000345165.10:c.1053+57_1053+60dup (CCDC78) MANE Select	ENSP00000316851.5:n.1053+57_1053+60dup
ENST00000293889.10:c.1053+57_1053+60dup (CCDC78)	ENSP00000293889.6:n.1053+57_1053+60dup
ENST00000345165.8:c.599+57_599+60dup (CCDC78)
ENST00000463539.5:n.1375+57_1375+60dup (CCDC78)
ENST00000466708.5:n.1397+57_1397+60dup (CCDC78)
ENST00000478979.5:n.1588_1591dup (CCDC78)
ENST00000481804.5:n.2031+57_2031+60dup (CCDC78)
ENST00000482152.1:n.414+57_414+60dup (CCDC78)
ENST00000482878.5:n.1991_1994dup (CCDC78)
ENST00000485091.5:n.1206+57_1206+60dup (CCDC78)
ENST00000620831.4:c.-49-38586_-49-38583dup (MSLN)	ENSP00000482893.1:n.-49-38586_-49-38583dup
NM_001031737.2:c.1053+57_1053+60dup (CCDC78)	NP_001026907.2:n.1053+57_1053+60dup
XM_006720838.1:c.1275+57_1275+60dup (CCDC78)	XP_006720901.1:n.1275+57_1275+60dup
XM_006720843.2:c.1053+57_1053+60dup (CCDC78)	XP_006720906.1:n.1053+57_1053+60dup
XM_011522356.1:c.1500+57_1500+60dup (CCDC78)	XP_011520658.1:n.1500+57_1500+60dup
XM_011522357.1:c.1488+57_1488+60dup (CCDC78)	XP_011520659.1:n.1488+57_1488+60dup
XM_011522358.1:c.1500+57_1500+60dup (CCDC78)	XP_011520660.1:n.1500+57_1500+60dup
XM_011522359.1:c.1467+57_1467+60dup (CCDC78)	XP_011520661.1:n.1467+57_1467+60dup
XM_011522360.1:c.1455+57_1455+60dup (CCDC78)	XP_011520662.1:n.1455+57_1455+60dup
XM_011522361.1:c.1500+57_1500+60dup (CCDC78)	XP_011520663.1:n.1500+57_1500+60dup
XM_011522362.1:c.1500+57_1500+60dup (CCDC78)	XP_011520664.1:n.1500+57_1500+60dup
XM_011522363.1:c.1500+57_1500+60dup (CCDC78)	XP_011520665.1:n.1500+57_1500+60dup
XM_011522364.1:c.1500+57_1500+60dup (CCDC78)	XP_011520666.1:n.1500+57_1500+60dup
XM_011522365.1:c.1287+57_1287+60dup (CCDC78)	XP_011520667.1:n.1287+57_1287+60dup
XM_011522366.1:c.1278+57_1278+60dup (CCDC78)	XP_011520668.1:n.1278+57_1278+60dup
XM_011522367.1:c.1119+57_1119+60dup (CCDC78)	XP_011520669.1:n.1119+57_1119+60dup
XM_011522368.1:c.1107+57_1107+60dup (CCDC78)	XP_011520670.1:n.1107+57_1107+60dup
XM_011522369.1:c.1065+57_1065+60dup (CCDC78)	XP_011520671.1:n.1065+57_1065+60dup
XM_011522370.1:c.897+57_897+60dup (CCDC78)	XP_011520672.1:n.897+57_897+60dup
XM_011522371.1:c.612+57_612+60dup (CCDC78)	XP_011520673.1:n.612+57_612+60dup
XM_006720843.4:c.1053+57_1053+60dup (CCDC78)	XP_006720906.1:n.1053+57_1053+60dup
XM_011522358.2:c.1500+57_1500+60dup (CCDC78)	XP_011520660.1:n.1500+57_1500+60dup
XM_011522371.2:c.612+57_612+60dup (CCDC78)	XP_011520673.1:n.612+57_612+60dup
XM_017022929.1:c.1500+57_1500+60dup (CCDC78)	XP_016878418.1:n.1500+57_1500+60dup
XM_017022930.1:c.600+57_600+60dup (CCDC78)	XP_016878419.1:n.600+57_600+60dup
XM_017022931.1:c.-313_-310dup (CCDC78)	XP_016878420.1:n.-313_-310dup
XM_024450150.1:c.330+57_330+60dup (CCDC78)	XP_024305918.1:n.330+57_330+60dup
XR_001751835.1:n.1839+57_1839+60dup (CCDC78)
XR_001751836.1:n.1818+57_1818+60dup (CCDC78)
XR_001751837.1:n.1596+57_1596+60dup (CCDC78)
XR_001751838.1:n.1942+57_1942+60dup (CCDC78)
XR_001751839.1:n.1404+57_1404+60dup (CCDC78)
NM_001031737.3:c.1053+57_1053+60dup (CCDC78)	NP_001026907.2:n.1053+57_1053+60dup
NM_001378030.1:c.1053+57_1053+60dup (CCDC78) MANE Select	NP_001364959.1:n.1053+57_1053+60dup
NM_001378031.1:c.953+273_953+276dup (CCDC78)	NP_001364960.1:n.953+273_953+276dup
NM_001378033.1:c.486+57_486+60dup (CCDC78)	NP_001364962.1:n.486+57_486+60dup
NR_165382.1:n.1610+57_1610+60dup (CCDC78)
NR_165383.1:n.1256+57_1256+60dup (CCDC78)
NR_165384.1:n.1221+57_1221+60dup (CCDC78)
NR_165385.1:n.1321+57_1321+60dup (CCDC78)
NR_165386.1:n.1388+57_1388+60dup (CCDC78)