Canonical Allele Identifier: CA2630857393

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-724038-GCCAGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724039_724043del , CM000678.2:g.724039_724043del	GRCh38
NC_000016.9:g.774039_774043del , CM000678.1:g.774039_774043del	GRCh37
NC_000016.8:g.714040_714044del	NCBI36
NG_032932.1:g.7431_7435del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1596+63_1596+67del (CCDC78)
ENST00000345165.10:c.1053+63_1053+67del (CCDC78) MANE Select	ENSP00000316851.5:n.1053+63_1053+67del
ENST00000293889.10:c.1053+63_1053+67del (CCDC78)	ENSP00000293889.6:n.1053+63_1053+67del
ENST00000345165.8:c.599+63_599+67del (CCDC78)
ENST00000463539.5:n.1375+63_1375+67del (CCDC78)
ENST00000466708.5:n.1397+63_1397+67del (CCDC78)
ENST00000478979.5:n.1594_1598del (CCDC78)
ENST00000481804.5:n.2031+63_2031+67del (CCDC78)
ENST00000482152.1:n.414+63_414+67del (CCDC78)
ENST00000482878.5:n.1997_2001del (CCDC78)
ENST00000485091.5:n.1206+63_1206+67del (CCDC78)
ENST00000620831.4:c.-49-38593_-49-38589del (MSLN)	ENSP00000482893.1:n.-49-38593_-49-38589del
NM_001031737.2:c.1053+63_1053+67del (CCDC78)	NP_001026907.2:n.1053+63_1053+67del
XM_006720838.1:c.1275+63_1275+67del (CCDC78)	XP_006720901.1:n.1275+63_1275+67del
XM_006720843.2:c.1053+63_1053+67del (CCDC78)	XP_006720906.1:n.1053+63_1053+67del
XM_011522356.1:c.1500+63_1500+67del (CCDC78)	XP_011520658.1:n.1500+63_1500+67del
XM_011522357.1:c.1488+63_1488+67del (CCDC78)	XP_011520659.1:n.1488+63_1488+67del
XM_011522358.1:c.1500+63_1500+67del (CCDC78)	XP_011520660.1:n.1500+63_1500+67del
XM_011522359.1:c.1467+63_1467+67del (CCDC78)	XP_011520661.1:n.1467+63_1467+67del
XM_011522360.1:c.1455+63_1455+67del (CCDC78)	XP_011520662.1:n.1455+63_1455+67del
XM_011522361.1:c.1500+63_1500+67del (CCDC78)	XP_011520663.1:n.1500+63_1500+67del
XM_011522362.1:c.1500+63_1500+67del (CCDC78)	XP_011520664.1:n.1500+63_1500+67del
XM_011522363.1:c.1500+63_1500+67del (CCDC78)	XP_011520665.1:n.1500+63_1500+67del
XM_011522364.1:c.1500+63_1500+67del (CCDC78)	XP_011520666.1:n.1500+63_1500+67del
XM_011522365.1:c.1287+63_1287+67del (CCDC78)	XP_011520667.1:n.1287+63_1287+67del
XM_011522366.1:c.1278+63_1278+67del (CCDC78)	XP_011520668.1:n.1278+63_1278+67del
XM_011522367.1:c.1119+63_1119+67del (CCDC78)	XP_011520669.1:n.1119+63_1119+67del
XM_011522368.1:c.1107+63_1107+67del (CCDC78)	XP_011520670.1:n.1107+63_1107+67del
XM_011522369.1:c.1065+63_1065+67del (CCDC78)	XP_011520671.1:n.1065+63_1065+67del
XM_011522370.1:c.897+63_897+67del (CCDC78)	XP_011520672.1:n.897+63_897+67del
XM_011522371.1:c.612+63_612+67del (CCDC78)	XP_011520673.1:n.612+63_612+67del
XM_006720843.4:c.1053+63_1053+67del (CCDC78)	XP_006720906.1:n.1053+63_1053+67del
XM_011522358.2:c.1500+63_1500+67del (CCDC78)	XP_011520660.1:n.1500+63_1500+67del
XM_011522371.2:c.612+63_612+67del (CCDC78)	XP_011520673.1:n.612+63_612+67del
XM_017022929.1:c.1500+63_1500+67del (CCDC78)	XP_016878418.1:n.1500+63_1500+67del
XM_017022930.1:c.600+63_600+67del (CCDC78)	XP_016878419.1:n.600+63_600+67del
XM_017022931.1:c.-307_-303del (CCDC78)	XP_016878420.1:n.-307_-303del
XM_024450150.1:c.330+63_330+67del (CCDC78)	XP_024305918.1:n.330+63_330+67del
XR_001751835.1:n.1839+63_1839+67del (CCDC78)
XR_001751836.1:n.1818+63_1818+67del (CCDC78)
XR_001751837.1:n.1596+63_1596+67del (CCDC78)
XR_001751838.1:n.1942+63_1942+67del (CCDC78)
XR_001751839.1:n.1404+63_1404+67del (CCDC78)
NM_001031737.3:c.1053+63_1053+67del (CCDC78)	NP_001026907.2:n.1053+63_1053+67del
NM_001378030.1:c.1053+63_1053+67del (CCDC78) MANE Select	NP_001364959.1:n.1053+63_1053+67del
NM_001378031.1:c.953+279_953+283del (CCDC78)	NP_001364960.1:n.953+279_953+283del
NM_001378033.1:c.486+63_486+67del (CCDC78)	NP_001364962.1:n.486+63_486+67del
NR_165382.1:n.1610+63_1610+67del (CCDC78)
NR_165383.1:n.1256+63_1256+67del (CCDC78)
NR_165384.1:n.1221+63_1221+67del (CCDC78)
NR_165385.1:n.1321+63_1321+67del (CCDC78)
NR_165386.1:n.1388+63_1388+67del (CCDC78)