Canonical Allele Identifier: CA394098556

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.773935T>C (hg19) ; chr16:g.723935T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723935T>C , CM000678.2:g.723935T>C	GRCh38
NC_000016.9:g.773935T>C , CM000678.1:g.773935T>C	GRCh37
NC_000016.8:g.713936T>C	NCBI36
NG_032932.1:g.7539A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1598A>G (CCDC78)
ENST00000345165.10:c.1055A>G (CCDC78) MANE Select	ENSP00000316851.5:p.His352Arg
ENST00000293889.10:c.1055A>G (CCDC78)	ENSP00000293889.6:p.His352Arg
ENST00000345165.8:c.601A>G (CCDC78)
ENST00000463539.5:n.1377A>G (CCDC78)
ENST00000466708.5:n.1399A>G (CCDC78)
ENST00000478979.5:n.1702A>G (CCDC78)
ENST00000481804.5:n.2033A>G (CCDC78)
ENST00000482152.1:n.416A>G (CCDC78)
ENST00000482878.5:n.2105A>G (CCDC78)
ENST00000485091.5:n.1208A>G (CCDC78)
ENST00000620831.4:c.-49-38697T>C (MSLN)	ENSP00000482893.1:n.-49-38697T>C
NM_001031737.2:c.1055A>G (CCDC78)	NP_001026907.2:p.His352Arg
XM_006720838.1:c.1277A>G (CCDC78)	XP_006720901.1:p.His426Arg
XM_006720843.2:c.1055A>G (CCDC78)	XP_006720906.1:p.His352Arg
XM_011522356.1:c.1502A>G (CCDC78)	XP_011520658.1:p.His501Arg
XM_011522357.1:c.1490A>G (CCDC78)	XP_011520659.1:p.His497Arg
XM_011522358.1:c.1502A>G (CCDC78)	XP_011520660.1:p.His501Arg
XM_011522359.1:c.1469A>G (CCDC78)	XP_011520661.1:p.His490Arg
XM_011522360.1:c.1457A>G (CCDC78)	XP_011520662.1:p.His486Arg
XM_011522361.1:c.1502A>G (CCDC78)	XP_011520663.1:p.His501Arg
XM_011522362.1:c.1502A>G (CCDC78)	XP_011520664.1:p.His501Arg
XM_011522363.1:c.1502A>G (CCDC78)	XP_011520665.1:p.His501Arg
XM_011522364.1:c.1502A>G (CCDC78)	XP_011520666.1:p.His501Arg
XM_011522365.1:c.1289A>G (CCDC78)	XP_011520667.1:p.His430Arg
XM_011522366.1:c.1280A>G (CCDC78)	XP_011520668.1:p.His427Arg
XM_011522367.1:c.1121A>G (CCDC78)	XP_011520669.1:p.His374Arg
XM_011522368.1:c.1109A>G (CCDC78)	XP_011520670.1:p.His370Arg
XM_011522369.1:c.1067A>G (CCDC78)	XP_011520671.1:p.His356Arg
XM_011522370.1:c.899A>G (CCDC78)	XP_011520672.1:p.His300Arg
XM_011522371.1:c.614A>G (CCDC78)	XP_011520673.1:p.His205Arg
XM_006720843.4:c.1055A>G (CCDC78)	XP_006720906.1:p.His352Arg
XM_011522358.2:c.1502A>G (CCDC78)	XP_011520660.1:p.His501Arg
XM_011522371.2:c.614A>G (CCDC78)	XP_011520673.1:p.His205Arg
XM_017022929.1:c.1502A>G (CCDC78)	XP_016878418.1:p.His501Arg
XM_017022930.1:c.602A>G (CCDC78)	XP_016878419.1:p.His201Arg
XM_017022931.1:c.-199A>G (CCDC78)	XP_016878420.1:n.-199A>G
XM_024450150.1:c.332A>G (CCDC78)	XP_024305918.1:p.His111Arg
XR_001751835.1:n.1841A>G (CCDC78)
XR_001751836.1:n.1820A>G (CCDC78)
XR_001751837.1:n.1598A>G (CCDC78)
XR_001751838.1:n.1944A>G (CCDC78)
XR_001751839.1:n.1406A>G (CCDC78)
NM_001031737.3:c.1055A>G (CCDC78)	NP_001026907.2:p.His352Arg
NM_001378030.1:c.1055A>G (CCDC78) MANE Select	NP_001364959.1:p.His352Arg
NM_001378031.1:c.953+387A>G (CCDC78)	NP_001364960.1:n.953+387A>G
NM_001378033.1:c.488A>G (CCDC78)	NP_001364962.1:p.His163Arg
NR_165382.1:n.1612A>G (CCDC78)
NR_165383.1:n.1258A>G (CCDC78)
NR_165384.1:n.1223A>G (CCDC78)
NR_165385.1:n.1323A>G (CCDC78)
NR_165386.1:n.1390A>G (CCDC78)