Canonical Allele Identifier: CA394098434

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.773906G>C (hg19) ; chr16:g.723906G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723906G>C , CM000678.2:g.723906G>C	GRCh38
NC_000016.9:g.773906G>C , CM000678.1:g.773906G>C	GRCh37
NC_000016.8:g.713907G>C	NCBI36
NG_032932.1:g.7568C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1627C>G (CCDC78)
ENST00000345165.10:c.1084C>G (CCDC78) MANE Select	ENSP00000316851.5:p.Pro362Ala
ENST00000293889.10:c.1084C>G (CCDC78)	ENSP00000293889.6:p.Pro362Ala
ENST00000345165.8:c.630C>G (CCDC78)
ENST00000463539.5:n.1406C>G (CCDC78)
ENST00000466708.5:n.1428C>G (CCDC78)
ENST00000478979.5:n.1731C>G (CCDC78)
ENST00000481804.5:n.2062C>G (CCDC78)
ENST00000482152.1:n.445C>G (CCDC78)
ENST00000482878.5:n.2134C>G (CCDC78)
ENST00000485091.5:n.1237C>G (CCDC78)
ENST00000620831.4:c.-49-38726G>C (MSLN)	ENSP00000482893.1:n.-49-38726G>C
NM_001031737.2:c.1084C>G (CCDC78)	NP_001026907.2:p.Pro362Ala
XM_006720838.1:c.1306C>G (CCDC78)	XP_006720901.1:p.Pro436Ala
XM_006720843.2:c.1084C>G (CCDC78)	XP_006720906.1:p.Pro362Ala
XM_011522356.1:c.1531C>G (CCDC78)	XP_011520658.1:p.Pro511Ala
XM_011522357.1:c.1519C>G (CCDC78)	XP_011520659.1:p.Pro507Ala
XM_011522358.1:c.1531C>G (CCDC78)	XP_011520660.1:p.Pro511Ala
XM_011522359.1:c.1498C>G (CCDC78)	XP_011520661.1:p.Pro500Ala
XM_011522360.1:c.1486C>G (CCDC78)	XP_011520662.1:p.Pro496Ala
XM_011522361.1:c.1531C>G (CCDC78)	XP_011520663.1:p.Pro511Ala
XM_011522362.1:c.1531C>G (CCDC78)	XP_011520664.1:p.Pro511Ala
XM_011522363.1:c.1531C>G (CCDC78)	XP_011520665.1:p.Pro511Ala
XM_011522364.1:c.1531C>G (CCDC78)	XP_011520666.1:p.Pro511Ala
XM_011522365.1:c.1318C>G (CCDC78)	XP_011520667.1:p.Pro440Ala
XM_011522366.1:c.1309C>G (CCDC78)	XP_011520668.1:p.Pro437Ala
XM_011522367.1:c.1150C>G (CCDC78)	XP_011520669.1:p.Pro384Ala
XM_011522368.1:c.1138C>G (CCDC78)	XP_011520670.1:p.Pro380Ala
XM_011522369.1:c.1096C>G (CCDC78)	XP_011520671.1:p.Pro366Ala
XM_011522370.1:c.928C>G (CCDC78)	XP_011520672.1:p.Pro310Ala
XM_011522371.1:c.643C>G (CCDC78)	XP_011520673.1:p.Pro215Ala
XM_006720843.4:c.1084C>G (CCDC78)	XP_006720906.1:p.Pro362Ala
XM_011522358.2:c.1531C>G (CCDC78)	XP_011520660.1:p.Pro511Ala
XM_011522371.2:c.643C>G (CCDC78)	XP_011520673.1:p.Pro215Ala
XM_017022929.1:c.1531C>G (CCDC78)	XP_016878418.1:p.Pro511Ala
XM_017022930.1:c.631C>G (CCDC78)	XP_016878419.1:p.Pro211Ala
XM_017022931.1:c.-170C>G (CCDC78)	XP_016878420.1:n.-170C>G
XM_024450150.1:c.361C>G (CCDC78)	XP_024305918.1:p.Pro121Ala
XR_001751835.1:n.1870C>G (CCDC78)
XR_001751836.1:n.1849C>G (CCDC78)
XR_001751837.1:n.1627C>G (CCDC78)
XR_001751838.1:n.1973C>G (CCDC78)
XR_001751839.1:n.1435C>G (CCDC78)
NM_001031737.3:c.1084C>G (CCDC78)	NP_001026907.2:p.Pro362Ala
NM_001378030.1:c.1084C>G (CCDC78) MANE Select	NP_001364959.1:p.Pro362Ala
NM_001378031.1:c.953+416C>G (CCDC78)	NP_001364960.1:n.953+416C>G
NM_001378033.1:c.517C>G (CCDC78)	NP_001364962.1:p.Pro173Ala
NR_165382.1:n.1641C>G (CCDC78)
NR_165383.1:n.1287C>G (CCDC78)
NR_165384.1:n.1252C>G (CCDC78)
NR_165385.1:n.1352C>G (CCDC78)
NR_165386.1:n.1419C>G (CCDC78)