Canonical Allele Identifier: CA394098373

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.773884G>C (hg19) ; chr16:g.723884G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723884G>C , CM000678.2:g.723884G>C	GRCh38
NC_000016.9:g.773884G>C , CM000678.1:g.773884G>C	GRCh37
NC_000016.8:g.713885G>C	NCBI36
NG_032932.1:g.7590C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1649C>G (CCDC78)
ENST00000345165.10:c.1106C>G (CCDC78) MANE Select	ENSP00000316851.5:p.Ala369Gly
ENST00000293889.10:c.1106C>G (CCDC78)	ENSP00000293889.6:p.Ala369Gly
ENST00000345165.8:c.652C>G (CCDC78)
ENST00000463539.5:n.1428C>G (CCDC78)
ENST00000466708.5:n.1450C>G (CCDC78)
ENST00000478979.5:n.1753C>G (CCDC78)
ENST00000481804.5:n.2084C>G (CCDC78)
ENST00000482152.1:n.467C>G (CCDC78)
ENST00000482878.5:n.2156C>G (CCDC78)
ENST00000485091.5:n.1259C>G (CCDC78)
ENST00000620831.4:c.-49-38748G>C (MSLN)	ENSP00000482893.1:n.-49-38748G>C
NM_001031737.2:c.1106C>G (CCDC78)	NP_001026907.2:p.Ala369Gly
XM_006720838.1:c.1328C>G (CCDC78)	XP_006720901.1:p.Ala443Gly
XM_006720843.2:c.1106C>G (CCDC78)	XP_006720906.1:p.Ala369Gly
XM_011522356.1:c.1553C>G (CCDC78)	XP_011520658.1:p.Ala518Gly
XM_011522357.1:c.1541C>G (CCDC78)	XP_011520659.1:p.Ala514Gly
XM_011522358.1:c.1553C>G (CCDC78)	XP_011520660.1:p.Ala518Gly
XM_011522359.1:c.1520C>G (CCDC78)	XP_011520661.1:p.Ala507Gly
XM_011522360.1:c.1508C>G (CCDC78)	XP_011520662.1:p.Ala503Gly
XM_011522361.1:c.1553C>G (CCDC78)	XP_011520663.1:p.Ala518Gly
XM_011522362.1:c.1553C>G (CCDC78)	XP_011520664.1:p.Ala518Gly
XM_011522363.1:c.1553C>G (CCDC78)	XP_011520665.1:p.Ala518Gly
XM_011522364.1:c.1553C>G (CCDC78)	XP_011520666.1:p.Ala518Gly
XM_011522365.1:c.1340C>G (CCDC78)	XP_011520667.1:p.Ala447Gly
XM_011522366.1:c.1331C>G (CCDC78)	XP_011520668.1:p.Ala444Gly
XM_011522367.1:c.1172C>G (CCDC78)	XP_011520669.1:p.Ala391Gly
XM_011522368.1:c.1160C>G (CCDC78)	XP_011520670.1:p.Ala387Gly
XM_011522369.1:c.1118C>G (CCDC78)	XP_011520671.1:p.Ala373Gly
XM_011522370.1:c.950C>G (CCDC78)	XP_011520672.1:p.Ala317Gly
XM_011522371.1:c.665C>G (CCDC78)	XP_011520673.1:p.Ala222Gly
XM_006720843.4:c.1106C>G (CCDC78)	XP_006720906.1:p.Ala369Gly
XM_011522358.2:c.1553C>G (CCDC78)	XP_011520660.1:p.Ala518Gly
XM_011522371.2:c.665C>G (CCDC78)	XP_011520673.1:p.Ala222Gly
XM_017022929.1:c.1553C>G (CCDC78)	XP_016878418.1:p.Ala518Gly
XM_017022930.1:c.653C>G (CCDC78)	XP_016878419.1:p.Ala218Gly
XM_017022931.1:c.-148C>G (CCDC78)	XP_016878420.1:n.-148C>G
XM_024450150.1:c.383C>G (CCDC78)	XP_024305918.1:p.Ala128Gly
XR_001751835.1:n.1892C>G (CCDC78)
XR_001751836.1:n.1871C>G (CCDC78)
XR_001751837.1:n.1649C>G (CCDC78)
XR_001751838.1:n.1995C>G (CCDC78)
XR_001751839.1:n.1457C>G (CCDC78)
NM_001031737.3:c.1106C>G (CCDC78)	NP_001026907.2:p.Ala369Gly
NM_001378030.1:c.1106C>G (CCDC78) MANE Select	NP_001364959.1:p.Ala369Gly
NM_001378031.1:c.953+438C>G (CCDC78)	NP_001364960.1:n.953+438C>G
NM_001378033.1:c.539C>G (CCDC78)	NP_001364962.1:p.Ala180Gly
NR_165382.1:n.1663C>G (CCDC78)
NR_165383.1:n.1309C>G (CCDC78)
NR_165384.1:n.1274C>G (CCDC78)
NR_165385.1:n.1374C>G (CCDC78)
NR_165386.1:n.1441C>G (CCDC78)