Canonical Allele Identifier: CA2630856440

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-723896-CTCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723898_723900del , CM000678.2:g.723898_723900del	GRCh38
NC_000016.9:g.773898_773900del , CM000678.1:g.773898_773900del	GRCh37
NC_000016.8:g.713899_713901del	NCBI36
NG_032932.1:g.7575_7577del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1634_1636del (CCDC78)
ENST00000345165.10:c.1091_1093del (CCDC78) MANE Select	ENSP00000316851.5:p.Lys364del
ENST00000293889.10:c.1091_1093del (CCDC78)	ENSP00000293889.6:p.Lys364del
ENST00000345165.8:c.637_639del (CCDC78)
ENST00000463539.5:n.1413_1415del (CCDC78)
ENST00000466708.5:n.1435_1437del (CCDC78)
ENST00000478979.5:n.1738_1740del (CCDC78)
ENST00000481804.5:n.2069_2071del (CCDC78)
ENST00000482152.1:n.452_454del (CCDC78)
ENST00000482878.5:n.2141_2143del (CCDC78)
ENST00000485091.5:n.1244_1246del (CCDC78)
ENST00000620831.4:c.-49-38734_-49-38732del (MSLN)	ENSP00000482893.1:n.-49-38734_-49-38732del
NM_001031737.2:c.1091_1093del (CCDC78)	NP_001026907.2:p.Lys364del
XM_006720838.1:c.1313_1315del (CCDC78)	XP_006720901.1:p.Lys438del
XM_006720843.2:c.1091_1093del (CCDC78)	XP_006720906.1:p.Lys364del
XM_011522356.1:c.1538_1540del (CCDC78)	XP_011520658.1:p.Lys513del
XM_011522357.1:c.1526_1528del (CCDC78)	XP_011520659.1:p.Lys509del
XM_011522358.1:c.1538_1540del (CCDC78)	XP_011520660.1:p.Lys513del
XM_011522359.1:c.1505_1507del (CCDC78)	XP_011520661.1:p.Lys502del
XM_011522360.1:c.1493_1495del (CCDC78)	XP_011520662.1:p.Lys498del
XM_011522361.1:c.1538_1540del (CCDC78)	XP_011520663.1:p.Lys513del
XM_011522362.1:c.1538_1540del (CCDC78)	XP_011520664.1:p.Lys513del
XM_011522363.1:c.1538_1540del (CCDC78)	XP_011520665.1:p.Lys513del
XM_011522364.1:c.1538_1540del (CCDC78)	XP_011520666.1:p.Lys513del
XM_011522365.1:c.1325_1327del (CCDC78)	XP_011520667.1:p.Lys442del
XM_011522366.1:c.1316_1318del (CCDC78)	XP_011520668.1:p.Lys439del
XM_011522367.1:c.1157_1159del (CCDC78)	XP_011520669.1:p.Lys386del
XM_011522368.1:c.1145_1147del (CCDC78)	XP_011520670.1:p.Lys382del
XM_011522369.1:c.1103_1105del (CCDC78)	XP_011520671.1:p.Lys368del
XM_011522370.1:c.935_937del (CCDC78)	XP_011520672.1:p.Lys312del
XM_011522371.1:c.650_652del (CCDC78)	XP_011520673.1:p.Lys217del
XM_006720843.4:c.1091_1093del (CCDC78)	XP_006720906.1:p.Lys364del
XM_011522358.2:c.1538_1540del (CCDC78)	XP_011520660.1:p.Lys513del
XM_011522371.2:c.650_652del (CCDC78)	XP_011520673.1:p.Lys217del
XM_017022929.1:c.1538_1540del (CCDC78)	XP_016878418.1:p.Lys513del
XM_017022930.1:c.638_640del (CCDC78)	XP_016878419.1:p.Lys213del
XM_017022931.1:c.-163_-161del (CCDC78)	XP_016878420.1:n.-163_-161del
XM_024450150.1:c.368_370del (CCDC78)	XP_024305918.1:p.Lys123del
XR_001751835.1:n.1877_1879del (CCDC78)
XR_001751836.1:n.1856_1858del (CCDC78)
XR_001751837.1:n.1634_1636del (CCDC78)
XR_001751838.1:n.1980_1982del (CCDC78)
XR_001751839.1:n.1442_1444del (CCDC78)
NM_001031737.3:c.1091_1093del (CCDC78)	NP_001026907.2:p.Lys364del
NM_001378030.1:c.1091_1093del (CCDC78) MANE Select	NP_001364959.1:p.Lys364del
NM_001378031.1:c.953+423_953+425del (CCDC78)	NP_001364960.1:n.953+423_953+425del
NM_001378033.1:c.524_526del (CCDC78)	NP_001364962.1:p.Lys175del
NR_165382.1:n.1648_1650del (CCDC78)
NR_165383.1:n.1294_1296del (CCDC78)
NR_165384.1:n.1259_1261del (CCDC78)
NR_165385.1:n.1359_1361del (CCDC78)
NR_165386.1:n.1426_1428del (CCDC78)