Canonical Allele Identifier: CA2201211363

Gene: CCDC78 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723922C= , CM000678.2:g.723922C=	GRCh38
NC_000016.9:g.773922C= , CM000678.1:g.773922C=	GRCh37
NC_000016.8:g.713923C=	NCBI36
NG_032932.1:g.7552G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1611G= (CCDC78)
ENST00000345165.10:c.1068G= (CCDC78) MANE Select	ENSP00000316851.5:p.Gly356=
ENST00000293889.10:c.1068G= (CCDC78)	ENSP00000293889.6:p.Gly356=
ENST00000345165.8:c.614G= (CCDC78)
ENST00000463539.5:n.1390G= (CCDC78)
ENST00000466708.5:n.1412G= (CCDC78)
ENST00000478979.5:n.1715G= (CCDC78)
ENST00000481804.5:n.2046G= (CCDC78)
ENST00000482152.1:n.429G= (CCDC78)
ENST00000482878.5:n.2118G= (CCDC78)
ENST00000485091.5:n.1221G= (CCDC78)
ENST00000620831.4:c.-49-38710C= (MSLN)	ENSP00000482893.1:n.-49-38710C=
NM_001031737.2:c.1068G= (CCDC78)	NP_001026907.2:p.Gly356=
XM_006720838.1:c.1290G= (CCDC78)	XP_006720901.1:p.Gly430=
XM_006720843.2:c.1068G= (CCDC78)	XP_006720906.1:p.Gly356=
XM_011522356.1:c.1515G= (CCDC78)	XP_011520658.1:p.Gly505=
XM_011522357.1:c.1503G= (CCDC78)	XP_011520659.1:p.Gly501=
XM_011522358.1:c.1515G= (CCDC78)	XP_011520660.1:p.Gly505=
XM_011522359.1:c.1482G= (CCDC78)	XP_011520661.1:p.Gly494=
XM_011522360.1:c.1470G= (CCDC78)	XP_011520662.1:p.Gly490=
XM_011522361.1:c.1515G= (CCDC78)	XP_011520663.1:p.Gly505=
XM_011522362.1:c.1515G= (CCDC78)	XP_011520664.1:p.Gly505=
XM_011522363.1:c.1515G= (CCDC78)	XP_011520665.1:p.Gly505=
XM_011522364.1:c.1515G= (CCDC78)	XP_011520666.1:p.Gly505=
XM_011522365.1:c.1302G= (CCDC78)	XP_011520667.1:p.Gly434=
XM_011522366.1:c.1293G= (CCDC78)	XP_011520668.1:p.Gly431=
XM_011522367.1:c.1134G= (CCDC78)	XP_011520669.1:p.Gly378=
XM_011522368.1:c.1122G= (CCDC78)	XP_011520670.1:p.Gly374=
XM_011522369.1:c.1080G= (CCDC78)	XP_011520671.1:p.Gly360=
XM_011522370.1:c.912G= (CCDC78)	XP_011520672.1:p.Gly304=
XM_011522371.1:c.627G= (CCDC78)	XP_011520673.1:p.Gly209=
XM_006720843.4:c.1068G= (CCDC78)	XP_006720906.1:p.Gly356=
XM_011522358.2:c.1515G= (CCDC78)	XP_011520660.1:p.Gly505=
XM_011522371.2:c.627G= (CCDC78)	XP_011520673.1:p.Gly209=
XM_017022929.1:c.1515G= (CCDC78)	XP_016878418.1:p.Gly505=
XM_017022930.1:c.615G= (CCDC78)	XP_016878419.1:p.Gly205=
XM_017022931.1:c.-186G= (CCDC78)	XP_016878420.1:n.-186G=
XM_024450150.1:c.345G= (CCDC78)	XP_024305918.1:p.Gly115=
XR_001751835.1:n.1854G= (CCDC78)
XR_001751836.1:n.1833G= (CCDC78)
XR_001751837.1:n.1611G= (CCDC78)
XR_001751838.1:n.1957G= (CCDC78)
XR_001751839.1:n.1419G= (CCDC78)
NM_001031737.3:c.1068G= (CCDC78)	NP_001026907.2:p.Gly356=
NM_001378030.1:c.1068G= (CCDC78) MANE Select	NP_001364959.1:p.Gly356=
NM_001378031.1:c.953+400G= (CCDC78)	NP_001364960.1:n.953+400G=
NM_001378033.1:c.501G= (CCDC78)	NP_001364962.1:p.Gly167=
NR_165382.1:n.1625G= (CCDC78)
NR_165383.1:n.1271G= (CCDC78)
NR_165384.1:n.1236G= (CCDC78)
NR_165385.1:n.1336G= (CCDC78)
NR_165386.1:n.1403G= (CCDC78)