Canonical Allele Identifier: CA2630855131

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-723693-ACCCACG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723694_723699del , CM000678.2:g.723694_723699del	GRCh38
NC_000016.9:g.773694_773699del , CM000678.1:g.773694_773699del	GRCh37
NC_000016.8:g.713695_713700del	NCBI36
NG_032932.1:g.7775_7780del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1676+158_1676+163del (CCDC78)
ENST00000345165.10:c.1133+158_1133+163del (CCDC78) MANE Select	ENSP00000316851.5:n.1133+158_1133+163del
ENST00000293889.10:c.1133+158_1133+163del (CCDC78)	ENSP00000293889.6:n.1133+158_1133+163del
ENST00000345165.8:c.679+158_679+163del (CCDC78)
ENST00000463539.5:n.1455+158_1455+163del (CCDC78)
ENST00000466708.5:n.1477+158_1477+163del (CCDC78)
ENST00000478979.5:n.1938_1943del (CCDC78)
ENST00000481804.5:n.2269_2274del (CCDC78)
ENST00000482152.1:n.494+158_494+163del (CCDC78)
ENST00000482878.5:n.2341_2346del (CCDC78)
ENST00000485091.5:n.1286+158_1286+163del (CCDC78)
ENST00000620831.4:c.-49-38938_-49-38933del (MSLN)	ENSP00000482893.1:n.-49-38938_-49-38933del
NM_001031737.2:c.1133+158_1133+163del (CCDC78)	NP_001026907.2:n.1133+158_1133+163del
XM_006720838.1:c.1355+158_1355+163del (CCDC78)	XP_006720901.1:n.1355+158_1355+163del
XM_006720843.2:c.1133+158_1133+163del (CCDC78)	XP_006720906.1:n.1133+158_1133+163del
XM_011522356.1:c.1580+158_1580+163del (CCDC78)	XP_011520658.1:n.1580+158_1580+163del
XM_011522357.1:c.1568+158_1568+163del (CCDC78)	XP_011520659.1:n.1568+158_1568+163del
XM_011522358.1:c.1580+158_1580+163del (CCDC78)	XP_011520660.1:n.1580+158_1580+163del
XM_011522359.1:c.1547+158_1547+163del (CCDC78)	XP_011520661.1:n.1547+158_1547+163del
XM_011522360.1:c.1535+158_1535+163del (CCDC78)	XP_011520662.1:n.1535+158_1535+163del
XM_011522361.1:c.1580+158_1580+163del (CCDC78)	XP_011520663.1:n.1580+158_1580+163del
XM_011522362.1:c.1580+158_1580+163del (CCDC78)	XP_011520664.1:n.1580+158_1580+163del
XM_011522363.1:c.1580+158_1580+163del (CCDC78)	XP_011520665.1:n.1580+158_1580+163del
XM_011522364.1:c.1580+158_1580+163del (CCDC78)	XP_011520666.1:n.1580+158_1580+163del
XM_011522365.1:c.1367+158_1367+163del (CCDC78)	XP_011520667.1:n.1367+158_1367+163del
XM_011522366.1:c.1358+158_1358+163del (CCDC78)	XP_011520668.1:n.1358+158_1358+163del
XM_011522367.1:c.1199+158_1199+163del (CCDC78)	XP_011520669.1:n.1199+158_1199+163del
XM_011522368.1:c.1187+158_1187+163del (CCDC78)	XP_011520670.1:n.1187+158_1187+163del
XM_011522369.1:c.1145+158_1145+163del (CCDC78)	XP_011520671.1:n.1145+158_1145+163del
XM_011522370.1:c.977+158_977+163del (CCDC78)	XP_011520672.1:n.977+158_977+163del
XM_011522371.1:c.692+158_692+163del (CCDC78)	XP_011520673.1:n.692+158_692+163del
XM_006720843.4:c.1133+158_1133+163del (CCDC78)	XP_006720906.1:n.1133+158_1133+163del
XM_011522358.2:c.1580+158_1580+163del (CCDC78)	XP_011520660.1:n.1580+158_1580+163del
XM_011522371.2:c.692+158_692+163del (CCDC78)	XP_011520673.1:n.692+158_692+163del
XM_017022929.1:c.1580+158_1580+163del (CCDC78)	XP_016878418.1:n.1580+158_1580+163del
XM_017022930.1:c.680+158_680+163del (CCDC78)	XP_016878419.1:n.680+158_680+163del
XM_017022931.1:c.38_43del (CCDC78)	XP_016878420.1:p.Pro13_Val15delinsLeu
XM_024450150.1:c.410+158_410+163del (CCDC78)	XP_024305918.1:n.410+158_410+163del
XR_001751835.1:n.1919+158_1919+163del (CCDC78)
XR_001751836.1:n.1898+158_1898+163del (CCDC78)
XR_001751837.1:n.1676+158_1676+163del (CCDC78)
XR_001751838.1:n.2022+158_2022+163del (CCDC78)
XR_001751839.1:n.1484+158_1484+163del (CCDC78)
NM_001031737.3:c.1133+158_1133+163del (CCDC78)	NP_001026907.2:n.1133+158_1133+163del
NM_001378030.1:c.1133+158_1133+163del (CCDC78) MANE Select	NP_001364959.1:n.1133+158_1133+163del
NM_001378031.1:c.954-538_954-533del (CCDC78)	NP_001364960.1:n.954-538_954-533del
NM_001378033.1:c.566+158_566+163del (CCDC78)	NP_001364962.1:n.566+158_566+163del
NR_165382.1:n.1690+158_1690+163del (CCDC78)
NR_165383.1:n.1336+158_1336+163del (CCDC78)
NR_165384.1:n.1301+158_1301+163del (CCDC78)
NR_165385.1:n.1401+158_1401+163del (CCDC78)
NR_165386.1:n.1468+158_1468+163del (CCDC78)