Canonical Allele Identifier: CA2630857305

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-724031-GCCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724032_724034del , CM000678.2:g.724032_724034del	GRCh38
NC_000016.9:g.774032_774034del , CM000678.1:g.774032_774034del	GRCh37
NC_000016.8:g.714033_714035del	NCBI36
NG_032932.1:g.7440_7442del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1596+72_1596+74del (CCDC78)
ENST00000345165.10:c.1053+72_1053+74del (CCDC78) MANE Select	ENSP00000316851.5:n.1053+72_1053+74del
ENST00000293889.10:c.1053+72_1053+74del (CCDC78)	ENSP00000293889.6:n.1053+72_1053+74del
ENST00000345165.8:c.599+72_599+74del (CCDC78)
ENST00000463539.5:n.1375+72_1375+74del (CCDC78)
ENST00000466708.5:n.1397+72_1397+74del (CCDC78)
ENST00000478979.5:n.1603_1605del (CCDC78)
ENST00000481804.5:n.2031+72_2031+74del (CCDC78)
ENST00000482152.1:n.414+72_414+74del (CCDC78)
ENST00000482878.5:n.2006_2008del (CCDC78)
ENST00000485091.5:n.1206+72_1206+74del (CCDC78)
ENST00000620831.4:c.-49-38600_-49-38598del (MSLN)	ENSP00000482893.1:n.-49-38600_-49-38598del
NM_001031737.2:c.1053+72_1053+74del (CCDC78)	NP_001026907.2:n.1053+72_1053+74del
XM_006720838.1:c.1275+72_1275+74del (CCDC78)	XP_006720901.1:n.1275+72_1275+74del
XM_006720843.2:c.1053+72_1053+74del (CCDC78)	XP_006720906.1:n.1053+72_1053+74del
XM_011522356.1:c.1500+72_1500+74del (CCDC78)	XP_011520658.1:n.1500+72_1500+74del
XM_011522357.1:c.1488+72_1488+74del (CCDC78)	XP_011520659.1:n.1488+72_1488+74del
XM_011522358.1:c.1500+72_1500+74del (CCDC78)	XP_011520660.1:n.1500+72_1500+74del
XM_011522359.1:c.1467+72_1467+74del (CCDC78)	XP_011520661.1:n.1467+72_1467+74del
XM_011522360.1:c.1455+72_1455+74del (CCDC78)	XP_011520662.1:n.1455+72_1455+74del
XM_011522361.1:c.1500+72_1500+74del (CCDC78)	XP_011520663.1:n.1500+72_1500+74del
XM_011522362.1:c.1500+72_1500+74del (CCDC78)	XP_011520664.1:n.1500+72_1500+74del
XM_011522363.1:c.1500+72_1500+74del (CCDC78)	XP_011520665.1:n.1500+72_1500+74del
XM_011522364.1:c.1500+72_1500+74del (CCDC78)	XP_011520666.1:n.1500+72_1500+74del
XM_011522365.1:c.1287+72_1287+74del (CCDC78)	XP_011520667.1:n.1287+72_1287+74del
XM_011522366.1:c.1278+72_1278+74del (CCDC78)	XP_011520668.1:n.1278+72_1278+74del
XM_011522367.1:c.1119+72_1119+74del (CCDC78)	XP_011520669.1:n.1119+72_1119+74del
XM_011522368.1:c.1107+72_1107+74del (CCDC78)	XP_011520670.1:n.1107+72_1107+74del
XM_011522369.1:c.1065+72_1065+74del (CCDC78)	XP_011520671.1:n.1065+72_1065+74del
XM_011522370.1:c.897+72_897+74del (CCDC78)	XP_011520672.1:n.897+72_897+74del
XM_011522371.1:c.612+72_612+74del (CCDC78)	XP_011520673.1:n.612+72_612+74del
XM_006720843.4:c.1053+72_1053+74del (CCDC78)	XP_006720906.1:n.1053+72_1053+74del
XM_011522358.2:c.1500+72_1500+74del (CCDC78)	XP_011520660.1:n.1500+72_1500+74del
XM_011522371.2:c.612+72_612+74del (CCDC78)	XP_011520673.1:n.612+72_612+74del
XM_017022929.1:c.1500+72_1500+74del (CCDC78)	XP_016878418.1:n.1500+72_1500+74del
XM_017022930.1:c.600+72_600+74del (CCDC78)	XP_016878419.1:n.600+72_600+74del
XM_017022931.1:c.-298_-296del (CCDC78)	XP_016878420.1:n.-298_-296del
XM_024450150.1:c.330+72_330+74del (CCDC78)	XP_024305918.1:n.330+72_330+74del
XR_001751835.1:n.1839+72_1839+74del (CCDC78)
XR_001751836.1:n.1818+72_1818+74del (CCDC78)
XR_001751837.1:n.1596+72_1596+74del (CCDC78)
XR_001751838.1:n.1942+72_1942+74del (CCDC78)
XR_001751839.1:n.1404+72_1404+74del (CCDC78)
NM_001031737.3:c.1053+72_1053+74del (CCDC78)	NP_001026907.2:n.1053+72_1053+74del
NM_001378030.1:c.1053+72_1053+74del (CCDC78) MANE Select	NP_001364959.1:n.1053+72_1053+74del
NM_001378031.1:c.953+288_953+290del (CCDC78)	NP_001364960.1:n.953+288_953+290del
NM_001378033.1:c.486+72_486+74del (CCDC78)	NP_001364962.1:n.486+72_486+74del
NR_165382.1:n.1610+72_1610+74del (CCDC78)
NR_165383.1:n.1256+72_1256+74del (CCDC78)
NR_165384.1:n.1221+72_1221+74del (CCDC78)
NR_165385.1:n.1321+72_1321+74del (CCDC78)
NR_165386.1:n.1388+72_1388+74del (CCDC78)