Canonical Allele Identifier: CA394098369

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.773881G>T (hg19) ; chr16:g.723881G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723881G>T , CM000678.2:g.723881G>T	GRCh38
NC_000016.9:g.773881G>T , CM000678.1:g.773881G>T	GRCh37
NC_000016.8:g.713882G>T	NCBI36
NG_032932.1:g.7593C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1652C>A (CCDC78)
ENST00000345165.10:c.1109C>A (CCDC78) MANE Select	ENSP00000316851.5:p.Ser370Tyr
ENST00000293889.10:c.1109C>A (CCDC78)	ENSP00000293889.6:p.Ser370Tyr
ENST00000345165.8:c.655C>A (CCDC78)
ENST00000463539.5:n.1431C>A (CCDC78)
ENST00000466708.5:n.1453C>A (CCDC78)
ENST00000478979.5:n.1756C>A (CCDC78)
ENST00000481804.5:n.2087C>A (CCDC78)
ENST00000482152.1:n.470C>A (CCDC78)
ENST00000482878.5:n.2159C>A (CCDC78)
ENST00000485091.5:n.1262C>A (CCDC78)
ENST00000620831.4:c.-49-38751G>T (MSLN)	ENSP00000482893.1:n.-49-38751G>T
NM_001031737.2:c.1109C>A (CCDC78)	NP_001026907.2:p.Ser370Tyr
XM_006720838.1:c.1331C>A (CCDC78)	XP_006720901.1:p.Ser444Tyr
XM_006720843.2:c.1109C>A (CCDC78)	XP_006720906.1:p.Ser370Tyr
XM_011522356.1:c.1556C>A (CCDC78)	XP_011520658.1:p.Ser519Tyr
XM_011522357.1:c.1544C>A (CCDC78)	XP_011520659.1:p.Ser515Tyr
XM_011522358.1:c.1556C>A (CCDC78)	XP_011520660.1:p.Ser519Tyr
XM_011522359.1:c.1523C>A (CCDC78)	XP_011520661.1:p.Ser508Tyr
XM_011522360.1:c.1511C>A (CCDC78)	XP_011520662.1:p.Ser504Tyr
XM_011522361.1:c.1556C>A (CCDC78)	XP_011520663.1:p.Ser519Tyr
XM_011522362.1:c.1556C>A (CCDC78)	XP_011520664.1:p.Ser519Tyr
XM_011522363.1:c.1556C>A (CCDC78)	XP_011520665.1:p.Ser519Tyr
XM_011522364.1:c.1556C>A (CCDC78)	XP_011520666.1:p.Ser519Tyr
XM_011522365.1:c.1343C>A (CCDC78)	XP_011520667.1:p.Ser448Tyr
XM_011522366.1:c.1334C>A (CCDC78)	XP_011520668.1:p.Ser445Tyr
XM_011522367.1:c.1175C>A (CCDC78)	XP_011520669.1:p.Ser392Tyr
XM_011522368.1:c.1163C>A (CCDC78)	XP_011520670.1:p.Ser388Tyr
XM_011522369.1:c.1121C>A (CCDC78)	XP_011520671.1:p.Ser374Tyr
XM_011522370.1:c.953C>A (CCDC78)	XP_011520672.1:p.Ser318Tyr
XM_011522371.1:c.668C>A (CCDC78)	XP_011520673.1:p.Ser223Tyr
XM_006720843.4:c.1109C>A (CCDC78)	XP_006720906.1:p.Ser370Tyr
XM_011522358.2:c.1556C>A (CCDC78)	XP_011520660.1:p.Ser519Tyr
XM_011522371.2:c.668C>A (CCDC78)	XP_011520673.1:p.Ser223Tyr
XM_017022929.1:c.1556C>A (CCDC78)	XP_016878418.1:p.Ser519Tyr
XM_017022930.1:c.656C>A (CCDC78)	XP_016878419.1:p.Ser219Tyr
XM_017022931.1:c.-145C>A (CCDC78)	XP_016878420.1:n.-145C>A
XM_024450150.1:c.386C>A (CCDC78)	XP_024305918.1:p.Ser129Tyr
XR_001751835.1:n.1895C>A (CCDC78)
XR_001751836.1:n.1874C>A (CCDC78)
XR_001751837.1:n.1652C>A (CCDC78)
XR_001751838.1:n.1998C>A (CCDC78)
XR_001751839.1:n.1460C>A (CCDC78)
NM_001031737.3:c.1109C>A (CCDC78)	NP_001026907.2:p.Ser370Tyr
NM_001378030.1:c.1109C>A (CCDC78) MANE Select	NP_001364959.1:p.Ser370Tyr
NM_001378031.1:c.953+441C>A (CCDC78)	NP_001364960.1:n.953+441C>A
NM_001378033.1:c.542C>A (CCDC78)	NP_001364962.1:p.Ser181Tyr
NR_165382.1:n.1666C>A (CCDC78)
NR_165383.1:n.1312C>A (CCDC78)
NR_165384.1:n.1277C>A (CCDC78)
NR_165385.1:n.1377C>A (CCDC78)
NR_165386.1:n.1444C>A (CCDC78)