Canonical Allele Identifier: CA394098563

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.773936G>C (hg19) ; chr16:g.723936G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723936G>C , CM000678.2:g.723936G>C	GRCh38
NC_000016.9:g.773936G>C , CM000678.1:g.773936G>C	GRCh37
NC_000016.8:g.713937G>C	NCBI36
NG_032932.1:g.7538C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1597C>G (CCDC78)
ENST00000345165.10:c.1054C>G (CCDC78) MANE Select	ENSP00000316851.5:p.His352Asp
ENST00000293889.10:c.1054C>G (CCDC78)	ENSP00000293889.6:p.His352Asp
ENST00000345165.8:c.600C>G (CCDC78)
ENST00000463539.5:n.1376C>G (CCDC78)
ENST00000466708.5:n.1398C>G (CCDC78)
ENST00000478979.5:n.1701C>G (CCDC78)
ENST00000481804.5:n.2032C>G (CCDC78)
ENST00000482152.1:n.415C>G (CCDC78)
ENST00000482878.5:n.2104C>G (CCDC78)
ENST00000485091.5:n.1207C>G (CCDC78)
ENST00000620831.4:c.-49-38696G>C (MSLN)	ENSP00000482893.1:n.-49-38696G>C
NM_001031737.2:c.1054C>G (CCDC78)	NP_001026907.2:p.His352Asp
XM_006720838.1:c.1276C>G (CCDC78)	XP_006720901.1:p.His426Asp
XM_006720843.2:c.1054C>G (CCDC78)	XP_006720906.1:p.His352Asp
XM_011522356.1:c.1501C>G (CCDC78)	XP_011520658.1:p.His501Asp
XM_011522357.1:c.1489C>G (CCDC78)	XP_011520659.1:p.His497Asp
XM_011522358.1:c.1501C>G (CCDC78)	XP_011520660.1:p.His501Asp
XM_011522359.1:c.1468C>G (CCDC78)	XP_011520661.1:p.His490Asp
XM_011522360.1:c.1456C>G (CCDC78)	XP_011520662.1:p.His486Asp
XM_011522361.1:c.1501C>G (CCDC78)	XP_011520663.1:p.His501Asp
XM_011522362.1:c.1501C>G (CCDC78)	XP_011520664.1:p.His501Asp
XM_011522363.1:c.1501C>G (CCDC78)	XP_011520665.1:p.His501Asp
XM_011522364.1:c.1501C>G (CCDC78)	XP_011520666.1:p.His501Asp
XM_011522365.1:c.1288C>G (CCDC78)	XP_011520667.1:p.His430Asp
XM_011522366.1:c.1279C>G (CCDC78)	XP_011520668.1:p.His427Asp
XM_011522367.1:c.1120C>G (CCDC78)	XP_011520669.1:p.His374Asp
XM_011522368.1:c.1108C>G (CCDC78)	XP_011520670.1:p.His370Asp
XM_011522369.1:c.1066C>G (CCDC78)	XP_011520671.1:p.His356Asp
XM_011522370.1:c.898C>G (CCDC78)	XP_011520672.1:p.His300Asp
XM_011522371.1:c.613C>G (CCDC78)	XP_011520673.1:p.His205Asp
XM_006720843.4:c.1054C>G (CCDC78)	XP_006720906.1:p.His352Asp
XM_011522358.2:c.1501C>G (CCDC78)	XP_011520660.1:p.His501Asp
XM_011522371.2:c.613C>G (CCDC78)	XP_011520673.1:p.His205Asp
XM_017022929.1:c.1501C>G (CCDC78)	XP_016878418.1:p.His501Asp
XM_017022930.1:c.601C>G (CCDC78)	XP_016878419.1:p.His201Asp
XM_017022931.1:c.-200C>G (CCDC78)	XP_016878420.1:n.-200C>G
XM_024450150.1:c.331C>G (CCDC78)	XP_024305918.1:p.His111Asp
XR_001751835.1:n.1840C>G (CCDC78)
XR_001751836.1:n.1819C>G (CCDC78)
XR_001751837.1:n.1597C>G (CCDC78)
XR_001751838.1:n.1943C>G (CCDC78)
XR_001751839.1:n.1405C>G (CCDC78)
NM_001031737.3:c.1054C>G (CCDC78)	NP_001026907.2:p.His352Asp
NM_001378030.1:c.1054C>G (CCDC78) MANE Select	NP_001364959.1:p.His352Asp
NM_001378031.1:c.953+386C>G (CCDC78)	NP_001364960.1:n.953+386C>G
NM_001378033.1:c.487C>G (CCDC78)	NP_001364962.1:p.His163Asp
NR_165382.1:n.1611C>G (CCDC78)
NR_165383.1:n.1257C>G (CCDC78)
NR_165384.1:n.1222C>G (CCDC78)
NR_165385.1:n.1322C>G (CCDC78)
NR_165386.1:n.1389C>G (CCDC78)