Canonical Allele Identifier: CA2630857450

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-724039-CCAGTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724040_724044del , CM000678.2:g.724040_724044del	GRCh38
NC_000016.9:g.774040_774044del , CM000678.1:g.774040_774044del	GRCh37
NC_000016.8:g.714041_714045del	NCBI36
NG_032932.1:g.7430_7434del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1596+62_1596+66del (CCDC78)
ENST00000345165.10:c.1053+62_1053+66del (CCDC78) MANE Select	ENSP00000316851.5:n.1053+62_1053+66del
ENST00000293889.10:c.1053+62_1053+66del (CCDC78)	ENSP00000293889.6:n.1053+62_1053+66del
ENST00000345165.8:c.599+62_599+66del (CCDC78)
ENST00000463539.5:n.1375+62_1375+66del (CCDC78)
ENST00000466708.5:n.1397+62_1397+66del (CCDC78)
ENST00000478979.5:n.1593_1597del (CCDC78)
ENST00000481804.5:n.2031+62_2031+66del (CCDC78)
ENST00000482152.1:n.414+62_414+66del (CCDC78)
ENST00000482878.5:n.1996_2000del (CCDC78)
ENST00000485091.5:n.1206+62_1206+66del (CCDC78)
ENST00000620831.4:c.-49-38592_-49-38588del (MSLN)	ENSP00000482893.1:n.-49-38592_-49-38588del
NM_001031737.2:c.1053+62_1053+66del (CCDC78)	NP_001026907.2:n.1053+62_1053+66del
XM_006720838.1:c.1275+62_1275+66del (CCDC78)	XP_006720901.1:n.1275+62_1275+66del
XM_006720843.2:c.1053+62_1053+66del (CCDC78)	XP_006720906.1:n.1053+62_1053+66del
XM_011522356.1:c.1500+62_1500+66del (CCDC78)	XP_011520658.1:n.1500+62_1500+66del
XM_011522357.1:c.1488+62_1488+66del (CCDC78)	XP_011520659.1:n.1488+62_1488+66del
XM_011522358.1:c.1500+62_1500+66del (CCDC78)	XP_011520660.1:n.1500+62_1500+66del
XM_011522359.1:c.1467+62_1467+66del (CCDC78)	XP_011520661.1:n.1467+62_1467+66del
XM_011522360.1:c.1455+62_1455+66del (CCDC78)	XP_011520662.1:n.1455+62_1455+66del
XM_011522361.1:c.1500+62_1500+66del (CCDC78)	XP_011520663.1:n.1500+62_1500+66del
XM_011522362.1:c.1500+62_1500+66del (CCDC78)	XP_011520664.1:n.1500+62_1500+66del
XM_011522363.1:c.1500+62_1500+66del (CCDC78)	XP_011520665.1:n.1500+62_1500+66del
XM_011522364.1:c.1500+62_1500+66del (CCDC78)	XP_011520666.1:n.1500+62_1500+66del
XM_011522365.1:c.1287+62_1287+66del (CCDC78)	XP_011520667.1:n.1287+62_1287+66del
XM_011522366.1:c.1278+62_1278+66del (CCDC78)	XP_011520668.1:n.1278+62_1278+66del
XM_011522367.1:c.1119+62_1119+66del (CCDC78)	XP_011520669.1:n.1119+62_1119+66del
XM_011522368.1:c.1107+62_1107+66del (CCDC78)	XP_011520670.1:n.1107+62_1107+66del
XM_011522369.1:c.1065+62_1065+66del (CCDC78)	XP_011520671.1:n.1065+62_1065+66del
XM_011522370.1:c.897+62_897+66del (CCDC78)	XP_011520672.1:n.897+62_897+66del
XM_011522371.1:c.612+62_612+66del (CCDC78)	XP_011520673.1:n.612+62_612+66del
XM_006720843.4:c.1053+62_1053+66del (CCDC78)	XP_006720906.1:n.1053+62_1053+66del
XM_011522358.2:c.1500+62_1500+66del (CCDC78)	XP_011520660.1:n.1500+62_1500+66del
XM_011522371.2:c.612+62_612+66del (CCDC78)	XP_011520673.1:n.612+62_612+66del
XM_017022929.1:c.1500+62_1500+66del (CCDC78)	XP_016878418.1:n.1500+62_1500+66del
XM_017022930.1:c.600+62_600+66del (CCDC78)	XP_016878419.1:n.600+62_600+66del
XM_017022931.1:c.-308_-304del (CCDC78)	XP_016878420.1:n.-308_-304del
XM_024450150.1:c.330+62_330+66del (CCDC78)	XP_024305918.1:n.330+62_330+66del
XR_001751835.1:n.1839+62_1839+66del (CCDC78)
XR_001751836.1:n.1818+62_1818+66del (CCDC78)
XR_001751837.1:n.1596+62_1596+66del (CCDC78)
XR_001751838.1:n.1942+62_1942+66del (CCDC78)
XR_001751839.1:n.1404+62_1404+66del (CCDC78)
NM_001031737.3:c.1053+62_1053+66del (CCDC78)	NP_001026907.2:n.1053+62_1053+66del
NM_001378030.1:c.1053+62_1053+66del (CCDC78) MANE Select	NP_001364959.1:n.1053+62_1053+66del
NM_001378031.1:c.953+278_953+282del (CCDC78)	NP_001364960.1:n.953+278_953+282del
NM_001378033.1:c.486+62_486+66del (CCDC78)	NP_001364962.1:n.486+62_486+66del
NR_165382.1:n.1610+62_1610+66del (CCDC78)
NR_165383.1:n.1256+62_1256+66del (CCDC78)
NR_165384.1:n.1221+62_1221+66del (CCDC78)
NR_165385.1:n.1321+62_1321+66del (CCDC78)
NR_165386.1:n.1388+62_1388+66del (CCDC78)