Canonical Allele Identifier: CA394098392

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.773895T>G (hg19) ; chr16:g.723895T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723895T>G , CM000678.2:g.723895T>G	GRCh38
NC_000016.9:g.773895T>G , CM000678.1:g.773895T>G	GRCh37
NC_000016.8:g.713896T>G	NCBI36
NG_032932.1:g.7579A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1638A>C (CCDC78)
ENST00000345165.10:c.1095A>C (CCDC78) MANE Select	ENSP00000316851.5:p.Arg365Ser
ENST00000293889.10:c.1095A>C (CCDC78)	ENSP00000293889.6:p.Arg365Ser
ENST00000345165.8:c.641A>C (CCDC78)
ENST00000463539.5:n.1417A>C (CCDC78)
ENST00000466708.5:n.1439A>C (CCDC78)
ENST00000478979.5:n.1742A>C (CCDC78)
ENST00000481804.5:n.2073A>C (CCDC78)
ENST00000482152.1:n.456A>C (CCDC78)
ENST00000482878.5:n.2145A>C (CCDC78)
ENST00000485091.5:n.1248A>C (CCDC78)
ENST00000620831.4:c.-49-38737T>G (MSLN)	ENSP00000482893.1:n.-49-38737T>G
NM_001031737.2:c.1095A>C (CCDC78)	NP_001026907.2:p.Arg365Ser
XM_006720838.1:c.1317A>C (CCDC78)	XP_006720901.1:p.Arg439Ser
XM_006720843.2:c.1095A>C (CCDC78)	XP_006720906.1:p.Arg365Ser
XM_011522356.1:c.1542A>C (CCDC78)	XP_011520658.1:p.Arg514Ser
XM_011522357.1:c.1530A>C (CCDC78)	XP_011520659.1:p.Arg510Ser
XM_011522358.1:c.1542A>C (CCDC78)	XP_011520660.1:p.Arg514Ser
XM_011522359.1:c.1509A>C (CCDC78)	XP_011520661.1:p.Arg503Ser
XM_011522360.1:c.1497A>C (CCDC78)	XP_011520662.1:p.Arg499Ser
XM_011522361.1:c.1542A>C (CCDC78)	XP_011520663.1:p.Arg514Ser
XM_011522362.1:c.1542A>C (CCDC78)	XP_011520664.1:p.Arg514Ser
XM_011522363.1:c.1542A>C (CCDC78)	XP_011520665.1:p.Arg514Ser
XM_011522364.1:c.1542A>C (CCDC78)	XP_011520666.1:p.Arg514Ser
XM_011522365.1:c.1329A>C (CCDC78)	XP_011520667.1:p.Arg443Ser
XM_011522366.1:c.1320A>C (CCDC78)	XP_011520668.1:p.Arg440Ser
XM_011522367.1:c.1161A>C (CCDC78)	XP_011520669.1:p.Arg387Ser
XM_011522368.1:c.1149A>C (CCDC78)	XP_011520670.1:p.Arg383Ser
XM_011522369.1:c.1107A>C (CCDC78)	XP_011520671.1:p.Arg369Ser
XM_011522370.1:c.939A>C (CCDC78)	XP_011520672.1:p.Arg313Ser
XM_011522371.1:c.654A>C (CCDC78)	XP_011520673.1:p.Arg218Ser
XM_006720843.4:c.1095A>C (CCDC78)	XP_006720906.1:p.Arg365Ser
XM_011522358.2:c.1542A>C (CCDC78)	XP_011520660.1:p.Arg514Ser
XM_011522371.2:c.654A>C (CCDC78)	XP_011520673.1:p.Arg218Ser
XM_017022929.1:c.1542A>C (CCDC78)	XP_016878418.1:p.Arg514Ser
XM_017022930.1:c.642A>C (CCDC78)	XP_016878419.1:p.Arg214Ser
XM_017022931.1:c.-159A>C (CCDC78)	XP_016878420.1:n.-159A>C
XM_024450150.1:c.372A>C (CCDC78)	XP_024305918.1:p.Arg124Ser
XR_001751835.1:n.1881A>C (CCDC78)
XR_001751836.1:n.1860A>C (CCDC78)
XR_001751837.1:n.1638A>C (CCDC78)
XR_001751838.1:n.1984A>C (CCDC78)
XR_001751839.1:n.1446A>C (CCDC78)
NM_001031737.3:c.1095A>C (CCDC78)	NP_001026907.2:p.Arg365Ser
NM_001378030.1:c.1095A>C (CCDC78) MANE Select	NP_001364959.1:p.Arg365Ser
NM_001378031.1:c.953+427A>C (CCDC78)	NP_001364960.1:n.953+427A>C
NM_001378033.1:c.528A>C (CCDC78)	NP_001364962.1:p.Arg176Ser
NR_165382.1:n.1652A>C (CCDC78)
NR_165383.1:n.1298A>C (CCDC78)
NR_165384.1:n.1263A>C (CCDC78)
NR_165385.1:n.1363A>C (CCDC78)
NR_165386.1:n.1430A>C (CCDC78)