Canonical Allele Identifier: CA492830101

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.774133G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724133G>C , CM000678.2:g.724133G>C	GRCh38
NC_000016.9:g.774133G>C , CM000678.1:g.774133G>C	GRCh37
NC_000016.8:g.714134G>C	NCBI36
NG_032932.1:g.7341C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1569C>G (CCDC78)
ENST00000345165.10:c.1026C>G (CCDC78) MANE Select	ENSP00000316851.5:p.Val342=
ENST00000293889.10:c.1026C>G (CCDC78)	ENSP00000293889.6:p.Val342=
ENST00000345165.8:c.572C>G (CCDC78)
ENST00000463539.5:n.1348C>G (CCDC78)
ENST00000466708.5:n.1370C>G (CCDC78)
ENST00000478979.5:n.1504C>G (CCDC78)
ENST00000481804.5:n.2004C>G (CCDC78)
ENST00000482152.1:n.387C>G (CCDC78)
ENST00000482878.5:n.1907C>G (CCDC78)
ENST00000485091.5:n.1179C>G (CCDC78)
ENST00000620831.4:c.-49-38499G>C (MSLN)	ENSP00000482893.1:n.-49-38499G>C
NM_001031737.2:c.1026C>G (CCDC78)	NP_001026907.2:p.Val342=
XM_006720838.1:c.1248C>G (CCDC78)	XP_006720901.1:p.Val416=
XM_006720843.2:c.1026C>G (CCDC78)	XP_006720906.1:p.Val342=
XM_011522356.1:c.1473C>G (CCDC78)	XP_011520658.1:p.Val491=
XM_011522357.1:c.1461C>G (CCDC78)	XP_011520659.1:p.Val487=
XM_011522358.1:c.1473C>G (CCDC78)	XP_011520660.1:p.Val491=
XM_011522359.1:c.1440C>G (CCDC78)	XP_011520661.1:p.Val480=
XM_011522360.1:c.1428C>G (CCDC78)	XP_011520662.1:p.Val476=
XM_011522361.1:c.1473C>G (CCDC78)	XP_011520663.1:p.Val491=
XM_011522362.1:c.1473C>G (CCDC78)	XP_011520664.1:p.Val491=
XM_011522363.1:c.1473C>G (CCDC78)	XP_011520665.1:p.Val491=
XM_011522364.1:c.1473C>G (CCDC78)	XP_011520666.1:p.Val491=
XM_011522365.1:c.1260C>G (CCDC78)	XP_011520667.1:p.Val420=
XM_011522366.1:c.1251C>G (CCDC78)	XP_011520668.1:p.Val417=
XM_011522367.1:c.1092C>G (CCDC78)	XP_011520669.1:p.Val364=
XM_011522368.1:c.1080C>G (CCDC78)	XP_011520670.1:p.Val360=
XM_011522369.1:c.1038C>G (CCDC78)	XP_011520671.1:p.Val346=
XM_011522370.1:c.870C>G (CCDC78)	XP_011520672.1:p.Val290=
XM_011522371.1:c.585C>G (CCDC78)	XP_011520673.1:p.Val195=
XM_006720843.4:c.1026C>G (CCDC78)	XP_006720906.1:p.Val342=
XM_011522358.2:c.1473C>G (CCDC78)	XP_011520660.1:p.Val491=
XM_011522371.2:c.585C>G (CCDC78)	XP_011520673.1:p.Val195=
XM_017022929.1:c.1473C>G (CCDC78)	XP_016878418.1:p.Val491=
XM_017022930.1:c.573C>G (CCDC78)	XP_016878419.1:p.Val191=
XM_024450150.1:c.303C>G (CCDC78)	XP_024305918.1:p.Val101=
XR_001751835.1:n.1812C>G (CCDC78)
XR_001751836.1:n.1791C>G (CCDC78)
XR_001751837.1:n.1569C>G (CCDC78)
XR_001751838.1:n.1915C>G (CCDC78)
XR_001751839.1:n.1377C>G (CCDC78)
NM_001031737.3:c.1026C>G (CCDC78)	NP_001026907.2:p.Val342=
NM_001378030.1:c.1026C>G (CCDC78) MANE Select	NP_001364959.1:p.Val342=
NM_001378031.1:c.953+189C>G (CCDC78)	NP_001364960.1:n.953+189C>G
NM_001378033.1:c.459C>G (CCDC78)	NP_001364962.1:p.Val153=
NR_165382.1:n.1583C>G (CCDC78)
NR_165383.1:n.1229C>G (CCDC78)
NR_165384.1:n.1194C>G (CCDC78)
NR_165385.1:n.1294C>G (CCDC78)
NR_165386.1:n.1361C>G (CCDC78)