Canonical Allele Identifier: CA2630857222

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-724022-CAGGA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724023_724026del , CM000678.2:g.724023_724026del	GRCh38
NC_000016.9:g.774023_774026del , CM000678.1:g.774023_774026del	GRCh37
NC_000016.8:g.714024_714027del	NCBI36
NG_032932.1:g.7448_7451del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1596+80_1596+83del (CCDC78)
ENST00000345165.10:c.1053+80_1053+83del (CCDC78) MANE Select	ENSP00000316851.5:n.1053+80_1053+83del
ENST00000293889.10:c.1053+80_1053+83del (CCDC78)	ENSP00000293889.6:n.1053+80_1053+83del
ENST00000345165.8:c.599+80_599+83del (CCDC78)
ENST00000463539.5:n.1375+80_1375+83del (CCDC78)
ENST00000466708.5:n.1397+80_1397+83del (CCDC78)
ENST00000478979.5:n.1611_1614del (CCDC78)
ENST00000481804.5:n.2031+80_2031+83del (CCDC78)
ENST00000482152.1:n.414+80_414+83del (CCDC78)
ENST00000482878.5:n.2014_2017del (CCDC78)
ENST00000485091.5:n.1206+80_1206+83del (CCDC78)
ENST00000620831.4:c.-49-38609_-49-38606del (MSLN)	ENSP00000482893.1:n.-49-38609_-49-38606del
NM_001031737.2:c.1053+80_1053+83del (CCDC78)	NP_001026907.2:n.1053+80_1053+83del
XM_006720838.1:c.1275+80_1275+83del (CCDC78)	XP_006720901.1:n.1275+80_1275+83del
XM_006720843.2:c.1053+80_1053+83del (CCDC78)	XP_006720906.1:n.1053+80_1053+83del
XM_011522356.1:c.1500+80_1500+83del (CCDC78)	XP_011520658.1:n.1500+80_1500+83del
XM_011522357.1:c.1488+80_1488+83del (CCDC78)	XP_011520659.1:n.1488+80_1488+83del
XM_011522358.1:c.1500+80_1500+83del (CCDC78)	XP_011520660.1:n.1500+80_1500+83del
XM_011522359.1:c.1467+80_1467+83del (CCDC78)	XP_011520661.1:n.1467+80_1467+83del
XM_011522360.1:c.1455+80_1455+83del (CCDC78)	XP_011520662.1:n.1455+80_1455+83del
XM_011522361.1:c.1500+80_1500+83del (CCDC78)	XP_011520663.1:n.1500+80_1500+83del
XM_011522362.1:c.1500+80_1500+83del (CCDC78)	XP_011520664.1:n.1500+80_1500+83del
XM_011522363.1:c.1500+80_1500+83del (CCDC78)	XP_011520665.1:n.1500+80_1500+83del
XM_011522364.1:c.1500+80_1500+83del (CCDC78)	XP_011520666.1:n.1500+80_1500+83del
XM_011522365.1:c.1287+80_1287+83del (CCDC78)	XP_011520667.1:n.1287+80_1287+83del
XM_011522366.1:c.1278+80_1278+83del (CCDC78)	XP_011520668.1:n.1278+80_1278+83del
XM_011522367.1:c.1119+80_1119+83del (CCDC78)	XP_011520669.1:n.1119+80_1119+83del
XM_011522368.1:c.1107+80_1107+83del (CCDC78)	XP_011520670.1:n.1107+80_1107+83del
XM_011522369.1:c.1065+80_1065+83del (CCDC78)	XP_011520671.1:n.1065+80_1065+83del
XM_011522370.1:c.897+80_897+83del (CCDC78)	XP_011520672.1:n.897+80_897+83del
XM_011522371.1:c.612+80_612+83del (CCDC78)	XP_011520673.1:n.612+80_612+83del
XM_006720843.4:c.1053+80_1053+83del (CCDC78)	XP_006720906.1:n.1053+80_1053+83del
XM_011522358.2:c.1500+80_1500+83del (CCDC78)	XP_011520660.1:n.1500+80_1500+83del
XM_011522371.2:c.612+80_612+83del (CCDC78)	XP_011520673.1:n.612+80_612+83del
XM_017022929.1:c.1500+80_1500+83del (CCDC78)	XP_016878418.1:n.1500+80_1500+83del
XM_017022930.1:c.600+80_600+83del (CCDC78)	XP_016878419.1:n.600+80_600+83del
XM_017022931.1:c.-290_-287del (CCDC78)	XP_016878420.1:n.-290_-287del
XM_024450150.1:c.330+80_330+83del (CCDC78)	XP_024305918.1:n.330+80_330+83del
XR_001751835.1:n.1839+80_1839+83del (CCDC78)
XR_001751836.1:n.1818+80_1818+83del (CCDC78)
XR_001751837.1:n.1596+80_1596+83del (CCDC78)
XR_001751838.1:n.1942+80_1942+83del (CCDC78)
XR_001751839.1:n.1404+80_1404+83del (CCDC78)
NM_001031737.3:c.1053+80_1053+83del (CCDC78)	NP_001026907.2:n.1053+80_1053+83del
NM_001378030.1:c.1053+80_1053+83del (CCDC78) MANE Select	NP_001364959.1:n.1053+80_1053+83del
NM_001378031.1:c.953+296_953+299del (CCDC78)	NP_001364960.1:n.953+296_953+299del
NM_001378033.1:c.486+80_486+83del (CCDC78)	NP_001364962.1:n.486+80_486+83del
NR_165382.1:n.1610+80_1610+83del (CCDC78)
NR_165383.1:n.1256+80_1256+83del (CCDC78)
NR_165384.1:n.1221+80_1221+83del (CCDC78)
NR_165385.1:n.1321+80_1321+83del (CCDC78)
NR_165386.1:n.1388+80_1388+83del (CCDC78)