Canonical Allele Identifier: CA7789624

Gene: CCDC78 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.725423T>C , CM000678.2:g.725423T>C	GRCh38
NC_000016.9:g.775423T>C , CM000678.1:g.775423T>C	GRCh37
NC_000016.8:g.715424T>C	NCBI36
NG_032932.1:g.6051A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001378030.1:c.425A>G (CCDC78) MANE Select	NP_001364959.1:p.His142Arg
ENST00000345165.10:c.425A>G (CCDC78) MANE Select	ENSP00000316851.5:p.His142Arg
NM_001031737.2:c.425A>G (CCDC78)	NP_001026907.2:p.His142Arg
NM_001031737.3:c.425A>G (CCDC78)	NP_001026907.2:p.His142Arg
NM_001378031.1:c.425A>G (CCDC78)	NP_001364960.1:p.His142Arg
NM_001378033.1:c.-18-130A>G (CCDC78)	NP_001364962.1:n.-18-130A>G
NR_165382.1:n.723A>G (CCDC78)
NR_165383.1:n.457A>G (CCDC78)
NR_165384.1:n.434+23A>G (CCDC78)
NR_165385.1:n.501A>G (CCDC78)
NR_165386.1:n.501A>G (CCDC78)
ENST00000293889.10:c.425A>G (CCDC78)	ENSP00000293889.6:p.His142Arg
ENST00000423653.5:c.-29A>G (CCDC78)	ENSP00000458590.1:n.-29A>G
ENST00000423653.6:n.470A>G (CCDC78)
ENST00000439619.6:n.502A>G (CCDC78)
ENST00000460023.5:n.402+23A>G (CCDC78)
ENST00000463539.5:n.488A>G (CCDC78)
ENST00000466708.5:n.608+23A>G (CCDC78)
ENST00000471861.5:n.531A>G (CCDC78)
ENST00000474647.1:n.336-130A>G (CCDC78)
ENST00000478979.5:n.344-130A>G (CCDC78)
ENST00000481804.5:n.714A>G (CCDC78)
ENST00000482878.5:n.736A>G (CCDC78)
ENST00000485091.5:n.487A>G (CCDC78)
ENST00000538176.5:n.495A>G (CCDC78)
ENST00000544996.1:n.231A>G (CCDC78)
ENST00000620831.4:c.-49-37209T>C (MSLN)	ENSP00000482893.1:n.-49-37209T>C
ENST00000682391.1:n.514A>G (CCDC78)
XM_005255106.3:c.402+23A>G (CCDC78)	XP_005255163.1:n.402+23A>G
XM_006720838.1:c.647A>G (CCDC78)	XP_006720901.1:p.His216Arg
XM_006720843.2:c.425A>G (CCDC78)	XP_006720906.1:p.His142Arg
XM_006720843.4:c.425A>G (CCDC78)	XP_006720906.1:p.His142Arg
XM_011522356.1:c.860A>G (CCDC78)	XP_011520658.1:p.His287Arg
XM_011522357.1:c.860A>G (CCDC78)	XP_011520659.1:p.His287Arg
XM_011522358.1:c.860A>G (CCDC78)	XP_011520660.1:p.His287Arg
XM_011522358.2:c.860A>G (CCDC78)	XP_011520660.1:p.His287Arg
XM_011522359.1:c.837+23A>G (CCDC78)	XP_011520661.1:n.837+23A>G
XM_011522360.1:c.837+23A>G (CCDC78)	XP_011520662.1:n.837+23A>G
XM_011522361.1:c.860A>G (CCDC78)	XP_011520663.1:p.His287Arg
XM_011522362.1:c.860A>G (CCDC78)	XP_011520664.1:p.His287Arg
XM_011522363.1:c.860A>G (CCDC78)	XP_011520665.1:p.His287Arg
XM_011522364.1:c.860A>G (CCDC78)	XP_011520666.1:p.His287Arg
XM_011522365.1:c.647A>G (CCDC78)	XP_011520667.1:p.His216Arg
XM_011522366.1:c.638A>G (CCDC78)	XP_011520668.1:p.His213Arg
XM_011522367.1:c.490-130A>G (CCDC78)	XP_011520669.1:n.490-130A>G
XM_011522368.1:c.490-130A>G (CCDC78)	XP_011520670.1:n.490-130A>G
XM_011522369.1:c.425A>G (CCDC78)	XP_011520671.1:p.His142Arg
XM_011522370.1:c.268-130A>G (CCDC78)	XP_011520672.1:n.268-130A>G
XM_011522371.1:c.-18-130A>G (CCDC78)	XP_011520673.1:n.-18-130A>G
XM_011522371.2:c.-18-130A>G (CCDC78)	XP_011520673.1:n.-18-130A>G
XM_017022929.1:c.860A>G (CCDC78)	XP_016878418.1:p.His287Arg
XM_017022930.1:c.-29A>G (CCDC78)	XP_016878419.1:n.-29A>G
XR_001751835.1:n.949A>G (CCDC78)
XR_001751836.1:n.736A>G (CCDC78)
XR_001751837.1:n.514A>G (CCDC78)
XR_001751838.1:n.870+23A>G (CCDC78)
XR_001751839.1:n.514A>G (CCDC78)