Canonical Allele Identifier: CA7789440

Gene: CCDC78 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724691C>T , CM000678.2:g.724691C>T	GRCh38
NC_000016.9:g.774691C>T , CM000678.1:g.774691C>T	GRCh37
NC_000016.8:g.714692C>T	NCBI36
NG_032932.1:g.6783G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001378030.1:c.755G>A (CCDC78) MANE Select	NP_001364959.1:p.Trp252Ter
ENST00000345165.10:c.755G>A (CCDC78) MANE Select	ENSP00000316851.5:p.Trp252Ter
NM_001031737.2:c.755G>A (CCDC78)	NP_001026907.2:p.Trp252Ter
NM_001031737.3:c.755G>A (CCDC78)	NP_001026907.2:p.Trp252Ter
NM_001378031.1:c.755G>A (CCDC78)	NP_001364960.1:p.Trp252Ter
NM_001378033.1:c.199-182G>A (CCDC78)	NP_001364962.1:n.199-182G>A
NR_165382.1:n.1141G>A (CCDC78)
NR_165383.1:n.787G>A (CCDC78)
NR_165384.1:n.752G>A (CCDC78)
NR_165385.1:n.1023G>A (CCDC78)
NR_165386.1:n.919G>A (CCDC78)
ENST00000293889.10:c.755G>A (CCDC78)	ENSP00000293889.6:p.Trp252Ter
ENST00000345165.8:c.301G>A (CCDC78)
ENST00000439619.6:n.923G>A (CCDC78)
ENST00000463539.5:n.906G>A (CCDC78)
ENST00000466708.5:n.928G>A (CCDC78)
ENST00000478979.5:n.946G>A (CCDC78)
ENST00000481804.5:n.1446G>A (CCDC78)
ENST00000482878.5:n.1349G>A (CCDC78)
ENST00000485091.5:n.908G>A (CCDC78)
ENST00000538176.5:n.1017G>A (CCDC78)
ENST00000620831.4:c.-49-37941C>T (MSLN)	ENSP00000482893.1:n.-49-37941C>T
ENST00000682391.1:n.1127G>A (CCDC78)
XM_005255106.3:c.*216G>A (CCDC78)	XP_005255163.1:n.*216G>A
XM_006720838.1:c.977G>A (CCDC78)	XP_006720901.1:p.Trp326Ter
XM_006720843.2:c.755G>A (CCDC78)	XP_006720906.1:p.Trp252Ter
XM_006720843.4:c.755G>A (CCDC78)	XP_006720906.1:p.Trp252Ter
XM_011522356.1:c.1202G>A (CCDC78)	XP_011520658.1:p.Trp401Ter
XM_011522357.1:c.1190G>A (CCDC78)	XP_011520659.1:p.Trp397Ter
XM_011522358.1:c.1202G>A (CCDC78)	XP_011520660.1:p.Trp401Ter
XM_011522358.2:c.1202G>A (CCDC78)	XP_011520660.1:p.Trp401Ter
XM_011522359.1:c.1169G>A (CCDC78)	XP_011520661.1:p.Trp390Ter
XM_011522360.1:c.1157G>A (CCDC78)	XP_011520662.1:p.Trp386Ter
XM_011522361.1:c.1202G>A (CCDC78)	XP_011520663.1:p.Trp401Ter
XM_011522362.1:c.1202G>A (CCDC78)	XP_011520664.1:p.Trp401Ter
XM_011522363.1:c.1202G>A (CCDC78)	XP_011520665.1:p.Trp401Ter
XM_011522364.1:c.1202G>A (CCDC78)	XP_011520666.1:p.Trp401Ter
XM_011522365.1:c.989G>A (CCDC78)	XP_011520667.1:p.Trp330Ter
XM_011522366.1:c.980G>A (CCDC78)	XP_011520668.1:p.Trp327Ter
XM_011522367.1:c.821G>A (CCDC78)	XP_011520669.1:p.Trp274Ter
XM_011522368.1:c.809G>A (CCDC78)	XP_011520670.1:p.Trp270Ter
XM_011522369.1:c.767G>A (CCDC78)	XP_011520671.1:p.Trp256Ter
XM_011522370.1:c.599G>A (CCDC78)	XP_011520672.1:p.Trp200Ter
XM_011522371.1:c.314G>A (CCDC78)	XP_011520673.1:p.Trp105Ter
XM_011522371.2:c.314G>A (CCDC78)	XP_011520673.1:p.Trp105Ter
XM_017022929.1:c.1202G>A (CCDC78)	XP_016878418.1:p.Trp401Ter
XM_017022930.1:c.302G>A (CCDC78)	XP_016878419.1:p.Trp101Ter
XM_024450150.1:c.-140G>A (CCDC78)	XP_024305918.1:n.-140G>A
XR_001751835.1:n.1370G>A (CCDC78)
XR_001751836.1:n.1349G>A (CCDC78)
XR_001751837.1:n.1127G>A (CCDC78)
XR_001751838.1:n.1473G>A (CCDC78)
XR_001751839.1:n.935G>A (CCDC78)