Canonical Allele Identifier: CA2201211483

Gene: CCDC78 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724108G= , CM000678.2:g.724108G=	GRCh38
NC_000016.9:g.774108G= , CM000678.1:g.774108G=	GRCh37
NC_000016.8:g.714109G=	NCBI36
NG_032932.1:g.7366C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1594C= (CCDC78)
ENST00000345165.10:c.1051C= (CCDC78) MANE Select	ENSP00000316851.5:p.Gln351=
ENST00000293889.10:c.1051C= (CCDC78)	ENSP00000293889.6:p.Gln351=
ENST00000345165.8:c.597C= (CCDC78)
ENST00000463539.5:n.1373C= (CCDC78)
ENST00000466708.5:n.1395C= (CCDC78)
ENST00000478979.5:n.1529C= (CCDC78)
ENST00000481804.5:n.2029C= (CCDC78)
ENST00000482152.1:n.412C= (CCDC78)
ENST00000482878.5:n.1932C= (CCDC78)
ENST00000485091.5:n.1204C= (CCDC78)
ENST00000620831.4:c.-49-38524G= (MSLN)	ENSP00000482893.1:n.-49-38524G=
NM_001031737.2:c.1051C= (CCDC78)	NP_001026907.2:p.Gln351=
XM_006720838.1:c.1273C= (CCDC78)	XP_006720901.1:p.Gln425=
XM_006720843.2:c.1051C= (CCDC78)	XP_006720906.1:p.Gln351=
XM_011522356.1:c.1498C= (CCDC78)	XP_011520658.1:p.Gln500=
XM_011522357.1:c.1486C= (CCDC78)	XP_011520659.1:p.Gln496=
XM_011522358.1:c.1498C= (CCDC78)	XP_011520660.1:p.Gln500=
XM_011522359.1:c.1465C= (CCDC78)	XP_011520661.1:p.Gln489=
XM_011522360.1:c.1453C= (CCDC78)	XP_011520662.1:p.Gln485=
XM_011522361.1:c.1498C= (CCDC78)	XP_011520663.1:p.Gln500=
XM_011522362.1:c.1498C= (CCDC78)	XP_011520664.1:p.Gln500=
XM_011522363.1:c.1498C= (CCDC78)	XP_011520665.1:p.Gln500=
XM_011522364.1:c.1498C= (CCDC78)	XP_011520666.1:p.Gln500=
XM_011522365.1:c.1285C= (CCDC78)	XP_011520667.1:p.Gln429=
XM_011522366.1:c.1276C= (CCDC78)	XP_011520668.1:p.Gln426=
XM_011522367.1:c.1117C= (CCDC78)	XP_011520669.1:p.Gln373=
XM_011522368.1:c.1105C= (CCDC78)	XP_011520670.1:p.Gln369=
XM_011522369.1:c.1063C= (CCDC78)	XP_011520671.1:p.Gln355=
XM_011522370.1:c.895C= (CCDC78)	XP_011520672.1:p.Gln299=
XM_011522371.1:c.610C= (CCDC78)	XP_011520673.1:p.Gln204=
XM_006720843.4:c.1051C= (CCDC78)	XP_006720906.1:p.Gln351=
XM_011522358.2:c.1498C= (CCDC78)	XP_011520660.1:p.Gln500=
XM_011522371.2:c.610C= (CCDC78)	XP_011520673.1:p.Gln204=
XM_017022929.1:c.1498C= (CCDC78)	XP_016878418.1:p.Gln500=
XM_017022930.1:c.598C= (CCDC78)	XP_016878419.1:p.Gln200=
XM_024450150.1:c.328C= (CCDC78)	XP_024305918.1:p.Gln110=
XR_001751835.1:n.1837C= (CCDC78)
XR_001751836.1:n.1816C= (CCDC78)
XR_001751837.1:n.1594C= (CCDC78)
XR_001751838.1:n.1940C= (CCDC78)
XR_001751839.1:n.1402C= (CCDC78)
NM_001031737.3:c.1051C= (CCDC78)	NP_001026907.2:p.Gln351=
NM_001378030.1:c.1051C= (CCDC78) MANE Select	NP_001364959.1:p.Gln351=
NM_001378031.1:c.953+214C= (CCDC78)	NP_001364960.1:n.953+214C=
NM_001378033.1:c.484C= (CCDC78)	NP_001364962.1:p.Gln162=
NR_165382.1:n.1608C= (CCDC78)
NR_165383.1:n.1254C= (CCDC78)
NR_165384.1:n.1219C= (CCDC78)
NR_165385.1:n.1319C= (CCDC78)
NR_165386.1:n.1386C= (CCDC78)