Canonical Allele Identifier: CA394098880

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.774140G>C (hg19) ; chr16:g.724140G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724140G>C , CM000678.2:g.724140G>C	GRCh38
NC_000016.9:g.774140G>C , CM000678.1:g.774140G>C	GRCh37
NC_000016.8:g.714141G>C	NCBI36
NG_032932.1:g.7334C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1562C>G (CCDC78)
ENST00000345165.10:c.1019C>G (CCDC78) MANE Select	ENSP00000316851.5:p.Pro340Arg
ENST00000293889.10:c.1019C>G (CCDC78)	ENSP00000293889.6:p.Pro340Arg
ENST00000345165.8:c.565C>G (CCDC78)
ENST00000463539.5:n.1341C>G (CCDC78)
ENST00000466708.5:n.1363C>G (CCDC78)
ENST00000478979.5:n.1497C>G (CCDC78)
ENST00000481804.5:n.1997C>G (CCDC78)
ENST00000482152.1:n.380C>G (CCDC78)
ENST00000482878.5:n.1900C>G (CCDC78)
ENST00000485091.5:n.1172C>G (CCDC78)
ENST00000620831.4:c.-49-38492G>C (MSLN)	ENSP00000482893.1:n.-49-38492G>C
NM_001031737.2:c.1019C>G (CCDC78)	NP_001026907.2:p.Pro340Arg
XM_006720838.1:c.1241C>G (CCDC78)	XP_006720901.1:p.Pro414Arg
XM_006720843.2:c.1019C>G (CCDC78)	XP_006720906.1:p.Pro340Arg
XM_011522356.1:c.1466C>G (CCDC78)	XP_011520658.1:p.Pro489Arg
XM_011522357.1:c.1454C>G (CCDC78)	XP_011520659.1:p.Pro485Arg
XM_011522358.1:c.1466C>G (CCDC78)	XP_011520660.1:p.Pro489Arg
XM_011522359.1:c.1433C>G (CCDC78)	XP_011520661.1:p.Pro478Arg
XM_011522360.1:c.1421C>G (CCDC78)	XP_011520662.1:p.Pro474Arg
XM_011522361.1:c.1466C>G (CCDC78)	XP_011520663.1:p.Pro489Arg
XM_011522362.1:c.1466C>G (CCDC78)	XP_011520664.1:p.Pro489Arg
XM_011522363.1:c.1466C>G (CCDC78)	XP_011520665.1:p.Pro489Arg
XM_011522364.1:c.1466C>G (CCDC78)	XP_011520666.1:p.Pro489Arg
XM_011522365.1:c.1253C>G (CCDC78)	XP_011520667.1:p.Pro418Arg
XM_011522366.1:c.1244C>G (CCDC78)	XP_011520668.1:p.Pro415Arg
XM_011522367.1:c.1085C>G (CCDC78)	XP_011520669.1:p.Pro362Arg
XM_011522368.1:c.1073C>G (CCDC78)	XP_011520670.1:p.Pro358Arg
XM_011522369.1:c.1031C>G (CCDC78)	XP_011520671.1:p.Pro344Arg
XM_011522370.1:c.863C>G (CCDC78)	XP_011520672.1:p.Pro288Arg
XM_011522371.1:c.578C>G (CCDC78)	XP_011520673.1:p.Pro193Arg
XM_006720843.4:c.1019C>G (CCDC78)	XP_006720906.1:p.Pro340Arg
XM_011522358.2:c.1466C>G (CCDC78)	XP_011520660.1:p.Pro489Arg
XM_011522371.2:c.578C>G (CCDC78)	XP_011520673.1:p.Pro193Arg
XM_017022929.1:c.1466C>G (CCDC78)	XP_016878418.1:p.Pro489Arg
XM_017022930.1:c.566C>G (CCDC78)	XP_016878419.1:p.Pro189Arg
XM_024450150.1:c.296C>G (CCDC78)	XP_024305918.1:p.Pro99Arg
XR_001751835.1:n.1805C>G (CCDC78)
XR_001751836.1:n.1784C>G (CCDC78)
XR_001751837.1:n.1562C>G (CCDC78)
XR_001751838.1:n.1908C>G (CCDC78)
XR_001751839.1:n.1370C>G (CCDC78)
NM_001031737.3:c.1019C>G (CCDC78)	NP_001026907.2:p.Pro340Arg
NM_001378030.1:c.1019C>G (CCDC78) MANE Select	NP_001364959.1:p.Pro340Arg
NM_001378031.1:c.953+182C>G (CCDC78)	NP_001364960.1:n.953+182C>G
NM_001378033.1:c.452C>G (CCDC78)	NP_001364962.1:p.Pro151Arg
NR_165382.1:n.1576C>G (CCDC78)
NR_165383.1:n.1222C>G (CCDC78)
NR_165384.1:n.1187C>G (CCDC78)
NR_165385.1:n.1287C>G (CCDC78)
NR_165386.1:n.1354C>G (CCDC78)