Canonical Allele Identifier: CA7789781

Gene: CCDC78 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.726345C>T , CM000678.2:g.726345C>T	GRCh38
NC_000016.9:g.776345C>T , CM000678.1:g.776345C>T	GRCh37
NC_000016.8:g.716346C>T	NCBI36
NG_032932.1:g.5129G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001378030.1:c.23G>A (CCDC78) MANE Select	NP_001364959.1:p.Gly8Asp
ENST00000345165.10:c.23G>A (CCDC78) MANE Select	ENSP00000316851.5:p.Gly8Asp
NM_001031737.2:c.23G>A (CCDC78)	NP_001026907.2:p.Gly8Asp
NM_001031737.3:c.23G>A (CCDC78)	NP_001026907.2:p.Gly8Asp
NM_001378031.1:c.23G>A (CCDC78)	NP_001364960.1:p.Gly8Asp
NM_001378033.1:c.-225-260G>A (CCDC78)	NP_001364962.1:n.-225-260G>A
NR_165382.1:n.99G>A (CCDC78)
NR_165383.1:n.93-260G>A (CCDC78)
NR_165384.1:n.93-260G>A (CCDC78)
NR_165385.1:n.99G>A (CCDC78)
NR_165386.1:n.99G>A (CCDC78)
ENST00000293889.10:c.23G>A (CCDC78)	ENSP00000293889.6:p.Gly8Asp
ENST00000423653.5:c.-393-260G>A (CCDC78)	ENSP00000458590.1:n.-393-260G>A
ENST00000423653.6:n.106-260G>A (CCDC78)
ENST00000439619.6:n.100G>A (CCDC78)
ENST00000460023.5:n.23G>A (CCDC78)
ENST00000463539.5:n.86G>A (CCDC78)
ENST00000466708.5:n.267-260G>A (CCDC78)
ENST00000471861.5:n.167-260G>A (CCDC78)
ENST00000474647.1:n.129-260G>A (CCDC78)
ENST00000478979.5:n.99G>A (CCDC78)
ENST00000481804.5:n.99G>A (CCDC78)
ENST00000482878.5:n.112G>A (CCDC78)
ENST00000485091.5:n.85G>A (CCDC78)
ENST00000538176.5:n.93G>A (CCDC78)
ENST00000620831.4:c.-49-36287C>T (MSLN)	ENSP00000482893.1:n.-49-36287C>T
ENST00000650995.1:c.23G>A (CCDC78)	ENSP00000498860.1:p.Gly8Asp
ENST00000682391.1:n.112G>A (CCDC78)
XM_005255106.3:c.23G>A (CCDC78)	XP_005255163.1:p.Gly8Asp
XM_006720838.1:c.23G>A (CCDC78)	XP_006720901.1:p.Gly8Asp
XM_006720843.2:c.23G>A (CCDC78)	XP_006720906.1:p.Gly8Asp
XM_006720843.4:c.23G>A (CCDC78)	XP_006720906.1:p.Gly8Asp
XM_011522356.1:c.23G>A (CCDC78)	XP_011520658.1:p.Gly8Asp
XM_011522357.1:c.23G>A (CCDC78)	XP_011520659.1:p.Gly8Asp
XM_011522358.1:c.23G>A (CCDC78)	XP_011520660.1:p.Gly8Asp
XM_011522358.2:c.23G>A (CCDC78)	XP_011520660.1:p.Gly8Asp
XM_011522359.1:c.23G>A (CCDC78)	XP_011520661.1:p.Gly8Asp
XM_011522360.1:c.23G>A (CCDC78)	XP_011520662.1:p.Gly8Asp
XM_011522361.1:c.23G>A (CCDC78)	XP_011520663.1:p.Gly8Asp
XM_011522362.1:c.23G>A (CCDC78)	XP_011520664.1:p.Gly8Asp
XM_011522363.1:c.23G>A (CCDC78)	XP_011520665.1:p.Gly8Asp
XM_011522364.1:c.23G>A (CCDC78)	XP_011520666.1:p.Gly8Asp
XM_011522365.1:c.23G>A (CCDC78)	XP_011520667.1:p.Gly8Asp
XM_011522366.1:c.23G>A (CCDC78)	XP_011520668.1:p.Gly8Asp
XM_011522367.1:c.23G>A (CCDC78)	XP_011520669.1:p.Gly8Asp
XM_011522368.1:c.23G>A (CCDC78)	XP_011520670.1:p.Gly8Asp
XM_011522369.1:c.23G>A (CCDC78)	XP_011520671.1:p.Gly8Asp
XM_011522370.1:c.23G>A (CCDC78)	XP_011520672.1:p.Gly8Asp
XM_011522371.1:c.-225-260G>A (CCDC78)	XP_011520673.1:n.-225-260G>A
XM_011522371.2:c.-225-260G>A (CCDC78)	XP_011520673.1:n.-225-260G>A
XM_017022929.1:c.23G>A (CCDC78)	XP_016878418.1:p.Gly8Asp
XM_017022930.1:c.-393-260G>A (CCDC78)	XP_016878419.1:n.-393-260G>A
XR_001751835.1:n.112G>A (CCDC78)
XR_001751836.1:n.112G>A (CCDC78)
XR_001751837.1:n.112G>A (CCDC78)
XR_001751838.1:n.491G>A (CCDC78)
XR_001751839.1:n.112G>A (CCDC78)