Canonical Allele Identifier: CA492830056

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-723895-T-C
• MyVariant Identifiers: chr16:g.773895T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723895T>C , CM000678.2:g.723895T>C	GRCh38
NC_000016.9:g.773895T>C , CM000678.1:g.773895T>C	GRCh37
NC_000016.8:g.713896T>C	NCBI36
NG_032932.1:g.7579A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1638A>G (CCDC78)
ENST00000345165.10:c.1095A>G (CCDC78) MANE Select	ENSP00000316851.5:p.Arg365=
ENST00000293889.10:c.1095A>G (CCDC78)	ENSP00000293889.6:p.Arg365=
ENST00000345165.8:c.641A>G (CCDC78)
ENST00000463539.5:n.1417A>G (CCDC78)
ENST00000466708.5:n.1439A>G (CCDC78)
ENST00000478979.5:n.1742A>G (CCDC78)
ENST00000481804.5:n.2073A>G (CCDC78)
ENST00000482152.1:n.456A>G (CCDC78)
ENST00000482878.5:n.2145A>G (CCDC78)
ENST00000485091.5:n.1248A>G (CCDC78)
ENST00000620831.4:c.-49-38737T>C (MSLN)	ENSP00000482893.1:n.-49-38737T>C
NM_001031737.2:c.1095A>G (CCDC78)	NP_001026907.2:p.Arg365=
XM_006720838.1:c.1317A>G (CCDC78)	XP_006720901.1:p.Arg439=
XM_006720843.2:c.1095A>G (CCDC78)	XP_006720906.1:p.Arg365=
XM_011522356.1:c.1542A>G (CCDC78)	XP_011520658.1:p.Arg514=
XM_011522357.1:c.1530A>G (CCDC78)	XP_011520659.1:p.Arg510=
XM_011522358.1:c.1542A>G (CCDC78)	XP_011520660.1:p.Arg514=
XM_011522359.1:c.1509A>G (CCDC78)	XP_011520661.1:p.Arg503=
XM_011522360.1:c.1497A>G (CCDC78)	XP_011520662.1:p.Arg499=
XM_011522361.1:c.1542A>G (CCDC78)	XP_011520663.1:p.Arg514=
XM_011522362.1:c.1542A>G (CCDC78)	XP_011520664.1:p.Arg514=
XM_011522363.1:c.1542A>G (CCDC78)	XP_011520665.1:p.Arg514=
XM_011522364.1:c.1542A>G (CCDC78)	XP_011520666.1:p.Arg514=
XM_011522365.1:c.1329A>G (CCDC78)	XP_011520667.1:p.Arg443=
XM_011522366.1:c.1320A>G (CCDC78)	XP_011520668.1:p.Arg440=
XM_011522367.1:c.1161A>G (CCDC78)	XP_011520669.1:p.Arg387=
XM_011522368.1:c.1149A>G (CCDC78)	XP_011520670.1:p.Arg383=
XM_011522369.1:c.1107A>G (CCDC78)	XP_011520671.1:p.Arg369=
XM_011522370.1:c.939A>G (CCDC78)	XP_011520672.1:p.Arg313=
XM_011522371.1:c.654A>G (CCDC78)	XP_011520673.1:p.Arg218=
XM_006720843.4:c.1095A>G (CCDC78)	XP_006720906.1:p.Arg365=
XM_011522358.2:c.1542A>G (CCDC78)	XP_011520660.1:p.Arg514=
XM_011522371.2:c.654A>G (CCDC78)	XP_011520673.1:p.Arg218=
XM_017022929.1:c.1542A>G (CCDC78)	XP_016878418.1:p.Arg514=
XM_017022930.1:c.642A>G (CCDC78)	XP_016878419.1:p.Arg214=
XM_017022931.1:c.-159A>G (CCDC78)	XP_016878420.1:n.-159A>G
XM_024450150.1:c.372A>G (CCDC78)	XP_024305918.1:p.Arg124=
XR_001751835.1:n.1881A>G (CCDC78)
XR_001751836.1:n.1860A>G (CCDC78)
XR_001751837.1:n.1638A>G (CCDC78)
XR_001751838.1:n.1984A>G (CCDC78)
XR_001751839.1:n.1446A>G (CCDC78)
NM_001031737.3:c.1095A>G (CCDC78)	NP_001026907.2:p.Arg365=
NM_001378030.1:c.1095A>G (CCDC78) MANE Select	NP_001364959.1:p.Arg365=
NM_001378031.1:c.953+427A>G (CCDC78)	NP_001364960.1:n.953+427A>G
NM_001378033.1:c.528A>G (CCDC78)	NP_001364962.1:p.Arg176=
NR_165382.1:n.1652A>G (CCDC78)
NR_165383.1:n.1298A>G (CCDC78)
NR_165384.1:n.1263A>G (CCDC78)
NR_165385.1:n.1363A>G (CCDC78)
NR_165386.1:n.1430A>G (CCDC78)