Canonical Allele Identifier: CA2630855199

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-723705-ACCCCAGGGTGGGGATGTGCCACTGAGTGCATTGCTGTGACCAGACCCTGTCTGGCGGGGGCTTGGTGGAGCAACTGGGGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723716_723795del , CM000678.2:g.723716_723795del	GRCh38
NC_000016.9:g.773716_773795del , CM000678.1:g.773716_773795del	GRCh37
NC_000016.8:g.713717_713796del	NCBI36
NG_032932.1:g.7689_7768del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1676+72_1676+151del (CCDC78)
ENST00000345165.10:c.1133+72_1133+151del (CCDC78) MANE Select	ENSP00000316851.5:n.1133+72_1133+151del
ENST00000293889.10:c.1133+72_1133+151del (CCDC78)	ENSP00000293889.6:n.1133+72_1133+151del
ENST00000345165.8:c.679+72_679+151del (CCDC78)
ENST00000463539.5:n.1455+72_1455+151del (CCDC78)
ENST00000466708.5:n.1477+72_1477+151del (CCDC78)
ENST00000478979.5:n.1852_1931del (CCDC78)
ENST00000481804.5:n.2183_2262del (CCDC78)
ENST00000482152.1:n.494+72_494+151del (CCDC78)
ENST00000482878.5:n.2255_2334del (CCDC78)
ENST00000485091.5:n.1286+72_1286+151del (CCDC78)
ENST00000620831.4:c.-49-38916_-49-38837del (MSLN)	ENSP00000482893.1:n.-49-38916_-49-38837del
NM_001031737.2:c.1133+72_1133+151del (CCDC78)	NP_001026907.2:n.1133+72_1133+151del
XM_006720838.1:c.1355+72_1355+151del (CCDC78)	XP_006720901.1:n.1355+72_1355+151del
XM_006720843.2:c.1133+72_1133+151del (CCDC78)	XP_006720906.1:n.1133+72_1133+151del
XM_011522356.1:c.1580+72_1580+151del (CCDC78)	XP_011520658.1:n.1580+72_1580+151del
XM_011522357.1:c.1568+72_1568+151del (CCDC78)	XP_011520659.1:n.1568+72_1568+151del
XM_011522358.1:c.1580+72_1580+151del (CCDC78)	XP_011520660.1:n.1580+72_1580+151del
XM_011522359.1:c.1547+72_1547+151del (CCDC78)	XP_011520661.1:n.1547+72_1547+151del
XM_011522360.1:c.1535+72_1535+151del (CCDC78)	XP_011520662.1:n.1535+72_1535+151del
XM_011522361.1:c.1580+72_1580+151del (CCDC78)	XP_011520663.1:n.1580+72_1580+151del
XM_011522362.1:c.1580+72_1580+151del (CCDC78)	XP_011520664.1:n.1580+72_1580+151del
XM_011522363.1:c.1580+72_1580+151del (CCDC78)	XP_011520665.1:n.1580+72_1580+151del
XM_011522364.1:c.1580+72_1580+151del (CCDC78)	XP_011520666.1:n.1580+72_1580+151del
XM_011522365.1:c.1367+72_1367+151del (CCDC78)	XP_011520667.1:n.1367+72_1367+151del
XM_011522366.1:c.1358+72_1358+151del (CCDC78)	XP_011520668.1:n.1358+72_1358+151del
XM_011522367.1:c.1199+72_1199+151del (CCDC78)	XP_011520669.1:n.1199+72_1199+151del
XM_011522368.1:c.1187+72_1187+151del (CCDC78)	XP_011520670.1:n.1187+72_1187+151del
XM_011522369.1:c.1145+72_1145+151del (CCDC78)	XP_011520671.1:n.1145+72_1145+151del
XM_011522370.1:c.977+72_977+151del (CCDC78)	XP_011520672.1:n.977+72_977+151del
XM_011522371.1:c.692+72_692+151del (CCDC78)	XP_011520673.1:n.692+72_692+151del
XM_006720843.4:c.1133+72_1133+151del (CCDC78)	XP_006720906.1:n.1133+72_1133+151del
XM_011522358.2:c.1580+72_1580+151del (CCDC78)	XP_011520660.1:n.1580+72_1580+151del
XM_011522371.2:c.692+72_692+151del (CCDC78)	XP_011520673.1:n.692+72_692+151del
XM_017022929.1:c.1580+72_1580+151del (CCDC78)	XP_016878418.1:n.1580+72_1580+151del
XM_017022930.1:c.680+72_680+151del (CCDC78)	XP_016878419.1:n.680+72_680+151del
XM_017022931.1:c.-49_31del (CCDC78)
XM_024450150.1:c.410+72_410+151del (CCDC78)	XP_024305918.1:n.410+72_410+151del
XR_001751835.1:n.1919+72_1919+151del (CCDC78)
XR_001751836.1:n.1898+72_1898+151del (CCDC78)
XR_001751837.1:n.1676+72_1676+151del (CCDC78)
XR_001751838.1:n.2022+72_2022+151del (CCDC78)
XR_001751839.1:n.1484+72_1484+151del (CCDC78)
NM_001031737.3:c.1133+72_1133+151del (CCDC78)	NP_001026907.2:n.1133+72_1133+151del
NM_001378030.1:c.1133+72_1133+151del (CCDC78) MANE Select	NP_001364959.1:n.1133+72_1133+151del
NM_001378031.1:c.953+537_954-545del (CCDC78)	NP_001364960.1:n.953+537_954-545del
NM_001378033.1:c.566+72_566+151del (CCDC78)	NP_001364962.1:n.566+72_566+151del
NR_165382.1:n.1690+72_1690+151del (CCDC78)
NR_165383.1:n.1336+72_1336+151del (CCDC78)
NR_165384.1:n.1301+72_1301+151del (CCDC78)
NR_165385.1:n.1401+72_1401+151del (CCDC78)
NR_165386.1:n.1468+72_1468+151del (CCDC78)