Canonical Allele Identifier: CA394098320

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.773864C>G (hg19) ; chr16:g.723864C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723864C>G , CM000678.2:g.723864C>G	GRCh38
NC_000016.9:g.773864C>G , CM000678.1:g.773864C>G	GRCh37
NC_000016.8:g.713865C>G	NCBI36
NG_032932.1:g.7610G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1669G>C (CCDC78)
ENST00000345165.10:c.1126G>C (CCDC78) MANE Select	ENSP00000316851.5:p.Glu376Gln
ENST00000293889.10:c.1126G>C (CCDC78)	ENSP00000293889.6:p.Glu376Gln
ENST00000345165.8:c.672G>C (CCDC78)
ENST00000463539.5:n.1448G>C (CCDC78)
ENST00000466708.5:n.1470G>C (CCDC78)
ENST00000478979.5:n.1773G>C (CCDC78)
ENST00000481804.5:n.2104G>C (CCDC78)
ENST00000482152.1:n.487G>C (CCDC78)
ENST00000482878.5:n.2176G>C (CCDC78)
ENST00000485091.5:n.1279G>C (CCDC78)
ENST00000620831.4:c.-49-38768C>G (MSLN)	ENSP00000482893.1:n.-49-38768C>G
NM_001031737.2:c.1126G>C (CCDC78)	NP_001026907.2:p.Glu376Gln
XM_006720838.1:c.1348G>C (CCDC78)	XP_006720901.1:p.Glu450Gln
XM_006720843.2:c.1126G>C (CCDC78)	XP_006720906.1:p.Glu376Gln
XM_011522356.1:c.1573G>C (CCDC78)	XP_011520658.1:p.Glu525Gln
XM_011522357.1:c.1561G>C (CCDC78)	XP_011520659.1:p.Glu521Gln
XM_011522358.1:c.1573G>C (CCDC78)	XP_011520660.1:p.Glu525Gln
XM_011522359.1:c.1540G>C (CCDC78)	XP_011520661.1:p.Glu514Gln
XM_011522360.1:c.1528G>C (CCDC78)	XP_011520662.1:p.Glu510Gln
XM_011522361.1:c.1573G>C (CCDC78)	XP_011520663.1:p.Glu525Gln
XM_011522362.1:c.1573G>C (CCDC78)	XP_011520664.1:p.Glu525Gln
XM_011522363.1:c.1573G>C (CCDC78)	XP_011520665.1:p.Glu525Gln
XM_011522364.1:c.1573G>C (CCDC78)	XP_011520666.1:p.Glu525Gln
XM_011522365.1:c.1360G>C (CCDC78)	XP_011520667.1:p.Glu454Gln
XM_011522366.1:c.1351G>C (CCDC78)	XP_011520668.1:p.Glu451Gln
XM_011522367.1:c.1192G>C (CCDC78)	XP_011520669.1:p.Glu398Gln
XM_011522368.1:c.1180G>C (CCDC78)	XP_011520670.1:p.Glu394Gln
XM_011522369.1:c.1138G>C (CCDC78)	XP_011520671.1:p.Glu380Gln
XM_011522370.1:c.970G>C (CCDC78)	XP_011520672.1:p.Glu324Gln
XM_011522371.1:c.685G>C (CCDC78)	XP_011520673.1:p.Glu229Gln
XM_006720843.4:c.1126G>C (CCDC78)	XP_006720906.1:p.Glu376Gln
XM_011522358.2:c.1573G>C (CCDC78)	XP_011520660.1:p.Glu525Gln
XM_011522371.2:c.685G>C (CCDC78)	XP_011520673.1:p.Glu229Gln
XM_017022929.1:c.1573G>C (CCDC78)	XP_016878418.1:p.Glu525Gln
XM_017022930.1:c.673G>C (CCDC78)	XP_016878419.1:p.Glu225Gln
XM_017022931.1:c.-128G>C (CCDC78)	XP_016878420.1:n.-128G>C
XM_024450150.1:c.403G>C (CCDC78)	XP_024305918.1:p.Glu135Gln
XR_001751835.1:n.1912G>C (CCDC78)
XR_001751836.1:n.1891G>C (CCDC78)
XR_001751837.1:n.1669G>C (CCDC78)
XR_001751838.1:n.2015G>C (CCDC78)
XR_001751839.1:n.1477G>C (CCDC78)
NM_001031737.3:c.1126G>C (CCDC78)	NP_001026907.2:p.Glu376Gln
NM_001378030.1:c.1126G>C (CCDC78) MANE Select	NP_001364959.1:p.Glu376Gln
NM_001378031.1:c.953+458G>C (CCDC78)	NP_001364960.1:n.953+458G>C
NM_001378033.1:c.559G>C (CCDC78)	NP_001364962.1:p.Glu187Gln
NR_165382.1:n.1683G>C (CCDC78)
NR_165383.1:n.1329G>C (CCDC78)
NR_165384.1:n.1294G>C (CCDC78)
NR_165385.1:n.1394G>C (CCDC78)
NR_165386.1:n.1461G>C (CCDC78)