Canonical Allele Identifier: CA2201211336

Gene: CCDC78 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723885C= , CM000678.2:g.723885C=	GRCh38
NC_000016.9:g.773885C= , CM000678.1:g.773885C=	GRCh37
NC_000016.8:g.713886C=	NCBI36
NG_032932.1:g.7589G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1648G= (CCDC78)
ENST00000345165.10:c.1105G= (CCDC78) MANE Select	ENSP00000316851.5:p.Ala369=
ENST00000293889.10:c.1105G= (CCDC78)	ENSP00000293889.6:p.Ala369=
ENST00000345165.8:c.651G= (CCDC78)
ENST00000463539.5:n.1427G= (CCDC78)
ENST00000466708.5:n.1449G= (CCDC78)
ENST00000478979.5:n.1752G= (CCDC78)
ENST00000481804.5:n.2083G= (CCDC78)
ENST00000482152.1:n.466G= (CCDC78)
ENST00000482878.5:n.2155G= (CCDC78)
ENST00000485091.5:n.1258G= (CCDC78)
ENST00000620831.4:c.-49-38747C= (MSLN)	ENSP00000482893.1:n.-49-38747C=
NM_001031737.2:c.1105G= (CCDC78)	NP_001026907.2:p.Ala369=
XM_006720838.1:c.1327G= (CCDC78)	XP_006720901.1:p.Ala443=
XM_006720843.2:c.1105G= (CCDC78)	XP_006720906.1:p.Ala369=
XM_011522356.1:c.1552G= (CCDC78)	XP_011520658.1:p.Ala518=
XM_011522357.1:c.1540G= (CCDC78)	XP_011520659.1:p.Ala514=
XM_011522358.1:c.1552G= (CCDC78)	XP_011520660.1:p.Ala518=
XM_011522359.1:c.1519G= (CCDC78)	XP_011520661.1:p.Ala507=
XM_011522360.1:c.1507G= (CCDC78)	XP_011520662.1:p.Ala503=
XM_011522361.1:c.1552G= (CCDC78)	XP_011520663.1:p.Ala518=
XM_011522362.1:c.1552G= (CCDC78)	XP_011520664.1:p.Ala518=
XM_011522363.1:c.1552G= (CCDC78)	XP_011520665.1:p.Ala518=
XM_011522364.1:c.1552G= (CCDC78)	XP_011520666.1:p.Ala518=
XM_011522365.1:c.1339G= (CCDC78)	XP_011520667.1:p.Ala447=
XM_011522366.1:c.1330G= (CCDC78)	XP_011520668.1:p.Ala444=
XM_011522367.1:c.1171G= (CCDC78)	XP_011520669.1:p.Ala391=
XM_011522368.1:c.1159G= (CCDC78)	XP_011520670.1:p.Ala387=
XM_011522369.1:c.1117G= (CCDC78)	XP_011520671.1:p.Ala373=
XM_011522370.1:c.949G= (CCDC78)	XP_011520672.1:p.Ala317=
XM_011522371.1:c.664G= (CCDC78)	XP_011520673.1:p.Ala222=
XM_006720843.4:c.1105G= (CCDC78)	XP_006720906.1:p.Ala369=
XM_011522358.2:c.1552G= (CCDC78)	XP_011520660.1:p.Ala518=
XM_011522371.2:c.664G= (CCDC78)	XP_011520673.1:p.Ala222=
XM_017022929.1:c.1552G= (CCDC78)	XP_016878418.1:p.Ala518=
XM_017022930.1:c.652G= (CCDC78)	XP_016878419.1:p.Ala218=
XM_017022931.1:c.-149G= (CCDC78)	XP_016878420.1:n.-149G=
XM_024450150.1:c.382G= (CCDC78)	XP_024305918.1:p.Ala128=
XR_001751835.1:n.1891G= (CCDC78)
XR_001751836.1:n.1870G= (CCDC78)
XR_001751837.1:n.1648G= (CCDC78)
XR_001751838.1:n.1994G= (CCDC78)
XR_001751839.1:n.1456G= (CCDC78)
NM_001031737.3:c.1105G= (CCDC78)	NP_001026907.2:p.Ala369=
NM_001378030.1:c.1105G= (CCDC78) MANE Select	NP_001364959.1:p.Ala369=
NM_001378031.1:c.953+437G= (CCDC78)	NP_001364960.1:n.953+437G=
NM_001378033.1:c.538G= (CCDC78)	NP_001364962.1:p.Ala180=
NR_165382.1:n.1662G= (CCDC78)
NR_165383.1:n.1308G= (CCDC78)
NR_165384.1:n.1273G= (CCDC78)
NR_165385.1:n.1373G= (CCDC78)
NR_165386.1:n.1440G= (CCDC78)