Canonical Allele Identifier: CA2201211369

Gene: CCDC78 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723929C= , CM000678.2:g.723929C=	GRCh38
NC_000016.9:g.773929C= , CM000678.1:g.773929C=	GRCh37
NC_000016.8:g.713930C=	NCBI36
NG_032932.1:g.7545G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1604G= (CCDC78)
ENST00000345165.10:c.1061G= (CCDC78) MANE Select	ENSP00000316851.5:p.Gly354=
ENST00000293889.10:c.1061G= (CCDC78)	ENSP00000293889.6:p.Gly354=
ENST00000345165.8:c.607G= (CCDC78)
ENST00000463539.5:n.1383G= (CCDC78)
ENST00000466708.5:n.1405G= (CCDC78)
ENST00000478979.5:n.1708G= (CCDC78)
ENST00000481804.5:n.2039G= (CCDC78)
ENST00000482152.1:n.422G= (CCDC78)
ENST00000482878.5:n.2111G= (CCDC78)
ENST00000485091.5:n.1214G= (CCDC78)
ENST00000620831.4:c.-49-38703C= (MSLN)	ENSP00000482893.1:n.-49-38703C=
NM_001031737.2:c.1061G= (CCDC78)	NP_001026907.2:p.Gly354=
XM_006720838.1:c.1283G= (CCDC78)	XP_006720901.1:p.Gly428=
XM_006720843.2:c.1061G= (CCDC78)	XP_006720906.1:p.Gly354=
XM_011522356.1:c.1508G= (CCDC78)	XP_011520658.1:p.Gly503=
XM_011522357.1:c.1496G= (CCDC78)	XP_011520659.1:p.Gly499=
XM_011522358.1:c.1508G= (CCDC78)	XP_011520660.1:p.Gly503=
XM_011522359.1:c.1475G= (CCDC78)	XP_011520661.1:p.Gly492=
XM_011522360.1:c.1463G= (CCDC78)	XP_011520662.1:p.Gly488=
XM_011522361.1:c.1508G= (CCDC78)	XP_011520663.1:p.Gly503=
XM_011522362.1:c.1508G= (CCDC78)	XP_011520664.1:p.Gly503=
XM_011522363.1:c.1508G= (CCDC78)	XP_011520665.1:p.Gly503=
XM_011522364.1:c.1508G= (CCDC78)	XP_011520666.1:p.Gly503=
XM_011522365.1:c.1295G= (CCDC78)	XP_011520667.1:p.Gly432=
XM_011522366.1:c.1286G= (CCDC78)	XP_011520668.1:p.Gly429=
XM_011522367.1:c.1127G= (CCDC78)	XP_011520669.1:p.Gly376=
XM_011522368.1:c.1115G= (CCDC78)	XP_011520670.1:p.Gly372=
XM_011522369.1:c.1073G= (CCDC78)	XP_011520671.1:p.Gly358=
XM_011522370.1:c.905G= (CCDC78)	XP_011520672.1:p.Gly302=
XM_011522371.1:c.620G= (CCDC78)	XP_011520673.1:p.Gly207=
XM_006720843.4:c.1061G= (CCDC78)	XP_006720906.1:p.Gly354=
XM_011522358.2:c.1508G= (CCDC78)	XP_011520660.1:p.Gly503=
XM_011522371.2:c.620G= (CCDC78)	XP_011520673.1:p.Gly207=
XM_017022929.1:c.1508G= (CCDC78)	XP_016878418.1:p.Gly503=
XM_017022930.1:c.608G= (CCDC78)	XP_016878419.1:p.Gly203=
XM_017022931.1:c.-193G= (CCDC78)	XP_016878420.1:n.-193G=
XM_024450150.1:c.338G= (CCDC78)	XP_024305918.1:p.Gly113=
XR_001751835.1:n.1847G= (CCDC78)
XR_001751836.1:n.1826G= (CCDC78)
XR_001751837.1:n.1604G= (CCDC78)
XR_001751838.1:n.1950G= (CCDC78)
XR_001751839.1:n.1412G= (CCDC78)
NM_001031737.3:c.1061G= (CCDC78)	NP_001026907.2:p.Gly354=
NM_001378030.1:c.1061G= (CCDC78) MANE Select	NP_001364959.1:p.Gly354=
NM_001378031.1:c.953+393G= (CCDC78)	NP_001364960.1:n.953+393G=
NM_001378033.1:c.494G= (CCDC78)	NP_001364962.1:p.Gly165=
NR_165382.1:n.1618G= (CCDC78)
NR_165383.1:n.1264G= (CCDC78)
NR_165384.1:n.1229G= (CCDC78)
NR_165385.1:n.1329G= (CCDC78)
NR_165386.1:n.1396G= (CCDC78)