Canonical Allele Identifier: CA2630858398

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-724061-T-TGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724063_724067dup , CM000678.2:g.724063_724067dup	GRCh38
NC_000016.9:g.774063_774067dup , CM000678.1:g.774063_774067dup	GRCh37
NC_000016.8:g.714064_714068dup	NCBI36
NG_032932.1:g.7408_7412dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1596+40_1596+44dup (CCDC78)
ENST00000345165.10:c.1053+40_1053+44dup (CCDC78) MANE Select	ENSP00000316851.5:n.1053+40_1053+44dup
ENST00000293889.10:c.1053+40_1053+44dup (CCDC78)	ENSP00000293889.6:n.1053+40_1053+44dup
ENST00000345165.8:c.599+40_599+44dup (CCDC78)
ENST00000463539.5:n.1375+40_1375+44dup (CCDC78)
ENST00000466708.5:n.1397+40_1397+44dup (CCDC78)
ENST00000478979.5:n.1571_1575dup (CCDC78)
ENST00000481804.5:n.2031+40_2031+44dup (CCDC78)
ENST00000482152.1:n.414+40_414+44dup (CCDC78)
ENST00000482878.5:n.1974_1978dup (CCDC78)
ENST00000485091.5:n.1206+40_1206+44dup (CCDC78)
ENST00000620831.4:c.-49-38569_-49-38565dup (MSLN)	ENSP00000482893.1:n.-49-38569_-49-38565dup
NM_001031737.2:c.1053+40_1053+44dup (CCDC78)	NP_001026907.2:n.1053+40_1053+44dup
XM_006720838.1:c.1275+40_1275+44dup (CCDC78)	XP_006720901.1:n.1275+40_1275+44dup
XM_006720843.2:c.1053+40_1053+44dup (CCDC78)	XP_006720906.1:n.1053+40_1053+44dup
XM_011522356.1:c.1500+40_1500+44dup (CCDC78)	XP_011520658.1:n.1500+40_1500+44dup
XM_011522357.1:c.1488+40_1488+44dup (CCDC78)	XP_011520659.1:n.1488+40_1488+44dup
XM_011522358.1:c.1500+40_1500+44dup (CCDC78)	XP_011520660.1:n.1500+40_1500+44dup
XM_011522359.1:c.1467+40_1467+44dup (CCDC78)	XP_011520661.1:n.1467+40_1467+44dup
XM_011522360.1:c.1455+40_1455+44dup (CCDC78)	XP_011520662.1:n.1455+40_1455+44dup
XM_011522361.1:c.1500+40_1500+44dup (CCDC78)	XP_011520663.1:n.1500+40_1500+44dup
XM_011522362.1:c.1500+40_1500+44dup (CCDC78)	XP_011520664.1:n.1500+40_1500+44dup
XM_011522363.1:c.1500+40_1500+44dup (CCDC78)	XP_011520665.1:n.1500+40_1500+44dup
XM_011522364.1:c.1500+40_1500+44dup (CCDC78)	XP_011520666.1:n.1500+40_1500+44dup
XM_011522365.1:c.1287+40_1287+44dup (CCDC78)	XP_011520667.1:n.1287+40_1287+44dup
XM_011522366.1:c.1278+40_1278+44dup (CCDC78)	XP_011520668.1:n.1278+40_1278+44dup
XM_011522367.1:c.1119+40_1119+44dup (CCDC78)	XP_011520669.1:n.1119+40_1119+44dup
XM_011522368.1:c.1107+40_1107+44dup (CCDC78)	XP_011520670.1:n.1107+40_1107+44dup
XM_011522369.1:c.1065+40_1065+44dup (CCDC78)	XP_011520671.1:n.1065+40_1065+44dup
XM_011522370.1:c.897+40_897+44dup (CCDC78)	XP_011520672.1:n.897+40_897+44dup
XM_011522371.1:c.612+40_612+44dup (CCDC78)	XP_011520673.1:n.612+40_612+44dup
XM_006720843.4:c.1053+40_1053+44dup (CCDC78)	XP_006720906.1:n.1053+40_1053+44dup
XM_011522358.2:c.1500+40_1500+44dup (CCDC78)	XP_011520660.1:n.1500+40_1500+44dup
XM_011522371.2:c.612+40_612+44dup (CCDC78)	XP_011520673.1:n.612+40_612+44dup
XM_017022929.1:c.1500+40_1500+44dup (CCDC78)	XP_016878418.1:n.1500+40_1500+44dup
XM_017022930.1:c.600+40_600+44dup (CCDC78)	XP_016878419.1:n.600+40_600+44dup
XM_017022931.1:c.-330_-326dup (CCDC78)	XP_016878420.1:n.-330_-326dup
XM_024450150.1:c.330+40_330+44dup (CCDC78)	XP_024305918.1:n.330+40_330+44dup
XR_001751835.1:n.1839+40_1839+44dup (CCDC78)
XR_001751836.1:n.1818+40_1818+44dup (CCDC78)
XR_001751837.1:n.1596+40_1596+44dup (CCDC78)
XR_001751838.1:n.1942+40_1942+44dup (CCDC78)
XR_001751839.1:n.1404+40_1404+44dup (CCDC78)
NM_001031737.3:c.1053+40_1053+44dup (CCDC78)	NP_001026907.2:n.1053+40_1053+44dup
NM_001378030.1:c.1053+40_1053+44dup (CCDC78) MANE Select	NP_001364959.1:n.1053+40_1053+44dup
NM_001378031.1:c.953+256_953+260dup (CCDC78)	NP_001364960.1:n.953+256_953+260dup
NM_001378033.1:c.486+40_486+44dup (CCDC78)	NP_001364962.1:n.486+40_486+44dup
NR_165382.1:n.1610+40_1610+44dup (CCDC78)
NR_165383.1:n.1256+40_1256+44dup (CCDC78)
NR_165384.1:n.1221+40_1221+44dup (CCDC78)
NR_165385.1:n.1321+40_1321+44dup (CCDC78)
NR_165386.1:n.1388+40_1388+44dup (CCDC78)