Canonical Allele Identifier: CA2630857890

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-724060-G-GCGGGGGGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724060_724061insCGGGGGGCC , CM000678.2:g.724060_724061insCGGGGGGCC	GRCh38
NC_000016.9:g.774060_774061insCGGGGGGCC , CM000678.1:g.774060_774061insCGGGGGGCC	GRCh37
NC_000016.8:g.714061_714062insCGGGGGGCC	NCBI36
NG_032932.1:g.7413_7414insGGCCCCCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1596+45_1596+46insGGCCCCCCG (CCDC78)
ENST00000345165.10:c.1053+45_1053+46insGGCCCCCCG (CCDC78) MANE Select	ENSP00000316851.5:n.1053+45_1053+46insGGCCCCCCG
ENST00000293889.10:c.1053+45_1053+46insGGCCCCCCG (CCDC78)	ENSP00000293889.6:n.1053+45_1053+46insGGCCCCCCG
ENST00000345165.8:c.599+45_599+46insGGCCCCCCG (CCDC78)
ENST00000463539.5:n.1375+45_1375+46insGGCCCCCCG (CCDC78)
ENST00000466708.5:n.1397+45_1397+46insGGCCCCCCG (CCDC78)
ENST00000478979.5:n.1576_1577insGGCCCCCCG (CCDC78)
ENST00000481804.5:n.2031+45_2031+46insGGCCCCCCG (CCDC78)
ENST00000482152.1:n.414+45_414+46insGGCCCCCCG (CCDC78)
ENST00000482878.5:n.1979_1980insGGCCCCCCG (CCDC78)
ENST00000485091.5:n.1206+45_1206+46insGGCCCCCCG (CCDC78)
ENST00000620831.4:c.-49-38572_-49-38571insCGGGGGGCC (MSLN)	ENSP00000482893.1:n.-49-38572_-49-38571insCGGGGGGCC
NM_001031737.2:c.1053+45_1053+46insGGCCCCCCG (CCDC78)	NP_001026907.2:n.1053+45_1053+46insGGCCCCCCG
XM_006720838.1:c.1275+45_1275+46insGGCCCCCCG (CCDC78)	XP_006720901.1:n.1275+45_1275+46insGGCCCCCCG
XM_006720843.2:c.1053+45_1053+46insGGCCCCCCG (CCDC78)	XP_006720906.1:n.1053+45_1053+46insGGCCCCCCG
XM_011522356.1:c.1500+45_1500+46insGGCCCCCCG (CCDC78)	XP_011520658.1:n.1500+45_1500+46insGGCCCCCCG
XM_011522357.1:c.1488+45_1488+46insGGCCCCCCG (CCDC78)	XP_011520659.1:n.1488+45_1488+46insGGCCCCCCG
XM_011522358.1:c.1500+45_1500+46insGGCCCCCCG (CCDC78)	XP_011520660.1:n.1500+45_1500+46insGGCCCCCCG
XM_011522359.1:c.1467+45_1467+46insGGCCCCCCG (CCDC78)	XP_011520661.1:n.1467+45_1467+46insGGCCCCCCG
XM_011522360.1:c.1455+45_1455+46insGGCCCCCCG (CCDC78)	XP_011520662.1:n.1455+45_1455+46insGGCCCCCCG
XM_011522361.1:c.1500+45_1500+46insGGCCCCCCG (CCDC78)	XP_011520663.1:n.1500+45_1500+46insGGCCCCCCG
XM_011522362.1:c.1500+45_1500+46insGGCCCCCCG (CCDC78)	XP_011520664.1:n.1500+45_1500+46insGGCCCCCCG
XM_011522363.1:c.1500+45_1500+46insGGCCCCCCG (CCDC78)	XP_011520665.1:n.1500+45_1500+46insGGCCCCCCG
XM_011522364.1:c.1500+45_1500+46insGGCCCCCCG (CCDC78)	XP_011520666.1:n.1500+45_1500+46insGGCCCCCCG
XM_011522365.1:c.1287+45_1287+46insGGCCCCCCG (CCDC78)	XP_011520667.1:n.1287+45_1287+46insGGCCCCCCG
XM_011522366.1:c.1278+45_1278+46insGGCCCCCCG (CCDC78)	XP_011520668.1:n.1278+45_1278+46insGGCCCCCCG
XM_011522367.1:c.1119+45_1119+46insGGCCCCCCG (CCDC78)	XP_011520669.1:n.1119+45_1119+46insGGCCCCCCG
XM_011522368.1:c.1107+45_1107+46insGGCCCCCCG (CCDC78)	XP_011520670.1:n.1107+45_1107+46insGGCCCCCCG
XM_011522369.1:c.1065+45_1065+46insGGCCCCCCG (CCDC78)	XP_011520671.1:n.1065+45_1065+46insGGCCCCCCG
XM_011522370.1:c.897+45_897+46insGGCCCCCCG (CCDC78)	XP_011520672.1:n.897+45_897+46insGGCCCCCCG
XM_011522371.1:c.612+45_612+46insGGCCCCCCG (CCDC78)	XP_011520673.1:n.612+45_612+46insGGCCCCCCG
XM_006720843.4:c.1053+45_1053+46insGGCCCCCCG (CCDC78)	XP_006720906.1:n.1053+45_1053+46insGGCCCCCCG
XM_011522358.2:c.1500+45_1500+46insGGCCCCCCG (CCDC78)	XP_011520660.1:n.1500+45_1500+46insGGCCCCCCG
XM_011522371.2:c.612+45_612+46insGGCCCCCCG (CCDC78)	XP_011520673.1:n.612+45_612+46insGGCCCCCCG
XM_017022929.1:c.1500+45_1500+46insGGCCCCCCG (CCDC78)	XP_016878418.1:n.1500+45_1500+46insGGCCCCCCG
XM_017022930.1:c.600+45_600+46insGGCCCCCCG (CCDC78)	XP_016878419.1:n.600+45_600+46insGGCCCCCCG
XM_017022931.1:c.-325_-324insGGCCCCCCG (CCDC78)	XP_016878420.1:n.-325_-324insGGCCCCCCG
XM_024450150.1:c.330+45_330+46insGGCCCCCCG (CCDC78)	XP_024305918.1:n.330+45_330+46insGGCCCCCCG
XR_001751835.1:n.1839+45_1839+46insGGCCCCCCG (CCDC78)
XR_001751836.1:n.1818+45_1818+46insGGCCCCCCG (CCDC78)
XR_001751837.1:n.1596+45_1596+46insGGCCCCCCG (CCDC78)
XR_001751838.1:n.1942+45_1942+46insGGCCCCCCG (CCDC78)
XR_001751839.1:n.1404+45_1404+46insGGCCCCCCG (CCDC78)
NM_001031737.3:c.1053+45_1053+46insGGCCCCCCG (CCDC78)	NP_001026907.2:n.1053+45_1053+46insGGCCCCCCG
NM_001378030.1:c.1053+45_1053+46insGGCCCCCCG (CCDC78) MANE Select	NP_001364959.1:n.1053+45_1053+46insGGCCCCCCG
NM_001378031.1:c.953+261_953+262insGGCCCCCCG (CCDC78)	NP_001364960.1:n.953+261_953+262insGGCCCCCCG
NM_001378033.1:c.486+45_486+46insGGCCCCCCG (CCDC78)	NP_001364962.1:n.486+45_486+46insGGCCCCCCG
NR_165382.1:n.1610+45_1610+46insGGCCCCCCG (CCDC78)
NR_165383.1:n.1256+45_1256+46insGGCCCCCCG (CCDC78)
NR_165384.1:n.1221+45_1221+46insGGCCCCCCG (CCDC78)
NR_165385.1:n.1321+45_1321+46insGGCCCCCCG (CCDC78)
NR_165386.1:n.1388+45_1388+46insGGCCCCCCG (CCDC78)