Canonical Allele Identifier: CA2201211334

Gene: CCDC78 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723877_723878delinsCT , CM000678.2:g.723877_723878delinsCT	GRCh38
NC_000016.9:g.773877_773878delinsCT , CM000678.1:g.773877_773878delinsCT	GRCh37
NC_000016.8:g.713878_713879delinsCT	NCBI36
NG_032932.1:g.7596_7597delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1655_1656delinsAG (CCDC78)
ENST00000345165.10:c.1112_1113delinsAG (CCDC78) MANE Select	ENSP00000316851.5:p.Gln371=
ENST00000293889.10:c.1112_1113delinsAG (CCDC78)	ENSP00000293889.6:p.Gln371=
ENST00000345165.8:c.658_659delinsAG (CCDC78)
ENST00000463539.5:n.1434_1435delinsAG (CCDC78)
ENST00000466708.5:n.1456_1457delinsAG (CCDC78)
ENST00000478979.5:n.1759_1760delinsAG (CCDC78)
ENST00000481804.5:n.2090_2091delinsAG (CCDC78)
ENST00000482152.1:n.473_474delinsAG (CCDC78)
ENST00000482878.5:n.2162_2163delinsAG (CCDC78)
ENST00000485091.5:n.1265_1266delinsAG (CCDC78)
ENST00000620831.4:c.-49-38755_-49-38754delinsCT (MSLN)	ENSP00000482893.1:n.-49-38755_-49-38754delinsCT
NM_001031737.2:c.1112_1113delinsAG (CCDC78)	NP_001026907.2:p.Gln371=
XM_006720838.1:c.1334_1335delinsAG (CCDC78)	XP_006720901.1:p.Gln445=
XM_006720843.2:c.1112_1113delinsAG (CCDC78)	XP_006720906.1:p.Gln371=
XM_011522356.1:c.1559_1560delinsAG (CCDC78)	XP_011520658.1:p.Gln520=
XM_011522357.1:c.1547_1548delinsAG (CCDC78)	XP_011520659.1:p.Gln516=
XM_011522358.1:c.1559_1560delinsAG (CCDC78)	XP_011520660.1:p.Gln520=
XM_011522359.1:c.1526_1527delinsAG (CCDC78)	XP_011520661.1:p.Gln509=
XM_011522360.1:c.1514_1515delinsAG (CCDC78)	XP_011520662.1:p.Gln505=
XM_011522361.1:c.1559_1560delinsAG (CCDC78)	XP_011520663.1:p.Gln520=
XM_011522362.1:c.1559_1560delinsAG (CCDC78)	XP_011520664.1:p.Gln520=
XM_011522363.1:c.1559_1560delinsAG (CCDC78)	XP_011520665.1:p.Gln520=
XM_011522364.1:c.1559_1560delinsAG (CCDC78)	XP_011520666.1:p.Gln520=
XM_011522365.1:c.1346_1347delinsAG (CCDC78)	XP_011520667.1:p.Gln449=
XM_011522366.1:c.1337_1338delinsAG (CCDC78)	XP_011520668.1:p.Gln446=
XM_011522367.1:c.1178_1179delinsAG (CCDC78)	XP_011520669.1:p.Gln393=
XM_011522368.1:c.1166_1167delinsAG (CCDC78)	XP_011520670.1:p.Gln389=
XM_011522369.1:c.1124_1125delinsAG (CCDC78)	XP_011520671.1:p.Gln375=
XM_011522370.1:c.956_957delinsAG (CCDC78)	XP_011520672.1:p.Gln319=
XM_011522371.1:c.671_672delinsAG (CCDC78)	XP_011520673.1:p.Gln224=
XM_006720843.4:c.1112_1113delinsAG (CCDC78)	XP_006720906.1:p.Gln371=
XM_011522358.2:c.1559_1560delinsAG (CCDC78)	XP_011520660.1:p.Gln520=
XM_011522371.2:c.671_672delinsAG (CCDC78)	XP_011520673.1:p.Gln224=
XM_017022929.1:c.1559_1560delinsAG (CCDC78)	XP_016878418.1:p.Gln520=
XM_017022930.1:c.659_660delinsAG (CCDC78)	XP_016878419.1:p.Gln220=
XM_017022931.1:c.-142_-141delinsAG (CCDC78)	XP_016878420.1:n.-142_-141delinsAG
XM_024450150.1:c.389_390delinsAG (CCDC78)	XP_024305918.1:p.Gln130=
XR_001751835.1:n.1898_1899delinsAG (CCDC78)
XR_001751836.1:n.1877_1878delinsAG (CCDC78)
XR_001751837.1:n.1655_1656delinsAG (CCDC78)
XR_001751838.1:n.2001_2002delinsAG (CCDC78)
XR_001751839.1:n.1463_1464delinsAG (CCDC78)
NM_001031737.3:c.1112_1113delinsAG (CCDC78)	NP_001026907.2:p.Gln371=
NM_001378030.1:c.1112_1113delinsAG (CCDC78) MANE Select	NP_001364959.1:p.Gln371=
NM_001378031.1:c.953+444_953+445delinsAG (CCDC78)	NP_001364960.1:n.953+444_953+445delinsAG
NM_001378033.1:c.545_546delinsAG (CCDC78)	NP_001364962.1:p.Gln182=
NR_165382.1:n.1669_1670delinsAG (CCDC78)
NR_165383.1:n.1315_1316delinsAG (CCDC78)
NR_165384.1:n.1280_1281delinsAG (CCDC78)
NR_165385.1:n.1380_1381delinsAG (CCDC78)
NR_165386.1:n.1447_1448delinsAG (CCDC78)