Canonical Allele Identifier: CA2201211340

Gene: CCDC78 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723889A= , CM000678.2:g.723889A=	GRCh38
NC_000016.9:g.773889A= , CM000678.1:g.773889A=	GRCh37
NC_000016.8:g.713890A=	NCBI36
NG_032932.1:g.7585T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1644T= (CCDC78)
ENST00000345165.10:c.1101T= (CCDC78) MANE Select	ENSP00000316851.5:p.Gly367=
ENST00000293889.10:c.1101T= (CCDC78)	ENSP00000293889.6:p.Gly367=
ENST00000345165.8:c.647T= (CCDC78)
ENST00000463539.5:n.1423T= (CCDC78)
ENST00000466708.5:n.1445T= (CCDC78)
ENST00000478979.5:n.1748T= (CCDC78)
ENST00000481804.5:n.2079T= (CCDC78)
ENST00000482152.1:n.462T= (CCDC78)
ENST00000482878.5:n.2151T= (CCDC78)
ENST00000485091.5:n.1254T= (CCDC78)
ENST00000620831.4:c.-49-38743A= (MSLN)	ENSP00000482893.1:n.-49-38743A=
NM_001031737.2:c.1101T= (CCDC78)	NP_001026907.2:p.Gly367=
XM_006720838.1:c.1323T= (CCDC78)	XP_006720901.1:p.Gly441=
XM_006720843.2:c.1101T= (CCDC78)	XP_006720906.1:p.Gly367=
XM_011522356.1:c.1548T= (CCDC78)	XP_011520658.1:p.Gly516=
XM_011522357.1:c.1536T= (CCDC78)	XP_011520659.1:p.Gly512=
XM_011522358.1:c.1548T= (CCDC78)	XP_011520660.1:p.Gly516=
XM_011522359.1:c.1515T= (CCDC78)	XP_011520661.1:p.Gly505=
XM_011522360.1:c.1503T= (CCDC78)	XP_011520662.1:p.Gly501=
XM_011522361.1:c.1548T= (CCDC78)	XP_011520663.1:p.Gly516=
XM_011522362.1:c.1548T= (CCDC78)	XP_011520664.1:p.Gly516=
XM_011522363.1:c.1548T= (CCDC78)	XP_011520665.1:p.Gly516=
XM_011522364.1:c.1548T= (CCDC78)	XP_011520666.1:p.Gly516=
XM_011522365.1:c.1335T= (CCDC78)	XP_011520667.1:p.Gly445=
XM_011522366.1:c.1326T= (CCDC78)	XP_011520668.1:p.Gly442=
XM_011522367.1:c.1167T= (CCDC78)	XP_011520669.1:p.Gly389=
XM_011522368.1:c.1155T= (CCDC78)	XP_011520670.1:p.Gly385=
XM_011522369.1:c.1113T= (CCDC78)	XP_011520671.1:p.Gly371=
XM_011522370.1:c.945T= (CCDC78)	XP_011520672.1:p.Gly315=
XM_011522371.1:c.660T= (CCDC78)	XP_011520673.1:p.Gly220=
XM_006720843.4:c.1101T= (CCDC78)	XP_006720906.1:p.Gly367=
XM_011522358.2:c.1548T= (CCDC78)	XP_011520660.1:p.Gly516=
XM_011522371.2:c.660T= (CCDC78)	XP_011520673.1:p.Gly220=
XM_017022929.1:c.1548T= (CCDC78)	XP_016878418.1:p.Gly516=
XM_017022930.1:c.648T= (CCDC78)	XP_016878419.1:p.Gly216=
XM_017022931.1:c.-153T= (CCDC78)	XP_016878420.1:n.-153T=
XM_024450150.1:c.378T= (CCDC78)	XP_024305918.1:p.Gly126=
XR_001751835.1:n.1887T= (CCDC78)
XR_001751836.1:n.1866T= (CCDC78)
XR_001751837.1:n.1644T= (CCDC78)
XR_001751838.1:n.1990T= (CCDC78)
XR_001751839.1:n.1452T= (CCDC78)
NM_001031737.3:c.1101T= (CCDC78)	NP_001026907.2:p.Gly367=
NM_001378030.1:c.1101T= (CCDC78) MANE Select	NP_001364959.1:p.Gly367=
NM_001378031.1:c.953+433T= (CCDC78)	NP_001364960.1:n.953+433T=
NM_001378033.1:c.534T= (CCDC78)	NP_001364962.1:p.Gly178=
NR_165382.1:n.1658T= (CCDC78)
NR_165383.1:n.1304T= (CCDC78)
NR_165384.1:n.1269T= (CCDC78)
NR_165385.1:n.1369T= (CCDC78)
NR_165386.1:n.1436T= (CCDC78)