Canonical Allele Identifier: CA2630857287

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-724029-AGGCCTGGGGCCAGTGTGGGGCAGTGGGTGGGTGGGGGGCACCCG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724037_724080del , CM000678.2:g.724037_724080del	GRCh38
NC_000016.9:g.774037_774080del , CM000678.1:g.774037_774080del	GRCh37
NC_000016.8:g.714038_714081del	NCBI36
NG_032932.1:g.7401_7444del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1596+33_1596+76del (CCDC78)
ENST00000345165.10:c.1053+33_1053+76del (CCDC78) MANE Select	ENSP00000316851.5:n.1053+33_1053+76del
ENST00000293889.10:c.1053+33_1053+76del (CCDC78)	ENSP00000293889.6:n.1053+33_1053+76del
ENST00000345165.8:c.599+33_599+76del (CCDC78)
ENST00000463539.5:n.1375+33_1375+76del (CCDC78)
ENST00000466708.5:n.1397+33_1397+76del (CCDC78)
ENST00000478979.5:n.1564_1607del (CCDC78)
ENST00000481804.5:n.2031+33_2031+76del (CCDC78)
ENST00000482152.1:n.414+33_414+76del (CCDC78)
ENST00000482878.5:n.1967_2010del (CCDC78)
ENST00000485091.5:n.1206+33_1206+76del (CCDC78)
ENST00000620831.4:c.-49-38595_-49-38552del (MSLN)	ENSP00000482893.1:n.-49-38595_-49-38552del
NM_001031737.2:c.1053+33_1053+76del (CCDC78)	NP_001026907.2:n.1053+33_1053+76del
XM_006720838.1:c.1275+33_1275+76del (CCDC78)	XP_006720901.1:n.1275+33_1275+76del
XM_006720843.2:c.1053+33_1053+76del (CCDC78)	XP_006720906.1:n.1053+33_1053+76del
XM_011522356.1:c.1500+33_1500+76del (CCDC78)	XP_011520658.1:n.1500+33_1500+76del
XM_011522357.1:c.1488+33_1488+76del (CCDC78)	XP_011520659.1:n.1488+33_1488+76del
XM_011522358.1:c.1500+33_1500+76del (CCDC78)	XP_011520660.1:n.1500+33_1500+76del
XM_011522359.1:c.1467+33_1467+76del (CCDC78)	XP_011520661.1:n.1467+33_1467+76del
XM_011522360.1:c.1455+33_1455+76del (CCDC78)	XP_011520662.1:n.1455+33_1455+76del
XM_011522361.1:c.1500+33_1500+76del (CCDC78)	XP_011520663.1:n.1500+33_1500+76del
XM_011522362.1:c.1500+33_1500+76del (CCDC78)	XP_011520664.1:n.1500+33_1500+76del
XM_011522363.1:c.1500+33_1500+76del (CCDC78)	XP_011520665.1:n.1500+33_1500+76del
XM_011522364.1:c.1500+33_1500+76del (CCDC78)	XP_011520666.1:n.1500+33_1500+76del
XM_011522365.1:c.1287+33_1287+76del (CCDC78)	XP_011520667.1:n.1287+33_1287+76del
XM_011522366.1:c.1278+33_1278+76del (CCDC78)	XP_011520668.1:n.1278+33_1278+76del
XM_011522367.1:c.1119+33_1119+76del (CCDC78)	XP_011520669.1:n.1119+33_1119+76del
XM_011522368.1:c.1107+33_1107+76del (CCDC78)	XP_011520670.1:n.1107+33_1107+76del
XM_011522369.1:c.1065+33_1065+76del (CCDC78)	XP_011520671.1:n.1065+33_1065+76del
XM_011522370.1:c.897+33_897+76del (CCDC78)	XP_011520672.1:n.897+33_897+76del
XM_011522371.1:c.612+33_612+76del (CCDC78)	XP_011520673.1:n.612+33_612+76del
XM_006720843.4:c.1053+33_1053+76del (CCDC78)	XP_006720906.1:n.1053+33_1053+76del
XM_011522358.2:c.1500+33_1500+76del (CCDC78)	XP_011520660.1:n.1500+33_1500+76del
XM_011522371.2:c.612+33_612+76del (CCDC78)	XP_011520673.1:n.612+33_612+76del
XM_017022929.1:c.1500+33_1500+76del (CCDC78)	XP_016878418.1:n.1500+33_1500+76del
XM_017022930.1:c.600+33_600+76del (CCDC78)	XP_016878419.1:n.600+33_600+76del
XM_017022931.1:c.-337_-294del (CCDC78)	XP_016878420.1:n.-337_-294del
XM_024450150.1:c.330+33_330+76del (CCDC78)	XP_024305918.1:n.330+33_330+76del
XR_001751835.1:n.1839+33_1839+76del (CCDC78)
XR_001751836.1:n.1818+33_1818+76del (CCDC78)
XR_001751837.1:n.1596+33_1596+76del (CCDC78)
XR_001751838.1:n.1942+33_1942+76del (CCDC78)
XR_001751839.1:n.1404+33_1404+76del (CCDC78)
NM_001031737.3:c.1053+33_1053+76del (CCDC78)	NP_001026907.2:n.1053+33_1053+76del
NM_001378030.1:c.1053+33_1053+76del (CCDC78) MANE Select	NP_001364959.1:n.1053+33_1053+76del
NM_001378031.1:c.953+249_953+292del (CCDC78)	NP_001364960.1:n.953+249_953+292del
NM_001378033.1:c.486+33_486+76del (CCDC78)	NP_001364962.1:n.486+33_486+76del
NR_165382.1:n.1610+33_1610+76del (CCDC78)
NR_165383.1:n.1256+33_1256+76del (CCDC78)
NR_165384.1:n.1221+33_1221+76del (CCDC78)
NR_165385.1:n.1321+33_1321+76del (CCDC78)
NR_165386.1:n.1388+33_1388+76del (CCDC78)