Canonical Allele Identifier: CA620309776

Gene: CCDC78 MSLN

Linked Data

• dbSNP Id: rs1446434743
• gnomAD v2: 16-773985-CCCCTCAGAGG-C
• MyVariant Identifiers: chr16:g.773986_773995del (hg19) ; chr16:g.723986_723995del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723989_723998del , CM000678.2:g.723989_723998del	GRCh38
NC_000016.9:g.773989_773998del , CM000678.1:g.773989_773998del	GRCh37
NC_000016.8:g.713990_713999del	NCBI36
NG_032932.1:g.7479_7488del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1597-59_1597-50del (CCDC78)
ENST00000345165.10:c.1054-59_1054-50del (CCDC78) MANE Select	ENSP00000316851.5:n.1054-59_1054-50del
ENST00000293889.10:c.1054-59_1054-50del (CCDC78)	ENSP00000293889.6:n.1054-59_1054-50del
ENST00000345165.8:c.600-59_600-50del (CCDC78)
ENST00000463539.5:n.1376-59_1376-50del (CCDC78)
ENST00000466708.5:n.1398-59_1398-50del (CCDC78)
ENST00000478979.5:n.1642_1651del (CCDC78)
ENST00000481804.5:n.2032-59_2032-50del (CCDC78)
ENST00000482152.1:n.415-59_415-50del (CCDC78)
ENST00000482878.5:n.2045_2054del (CCDC78)
ENST00000485091.5:n.1207-59_1207-50del (CCDC78)
ENST00000620831.4:c.-49-38643_-49-38634del (MSLN)	ENSP00000482893.1:n.-49-38643_-49-38634del
NM_001031737.2:c.1054-59_1054-50del (CCDC78)	NP_001026907.2:n.1054-59_1054-50del
XM_006720838.1:c.1276-59_1276-50del (CCDC78)	XP_006720901.1:n.1276-59_1276-50del
XM_006720843.2:c.1054-59_1054-50del (CCDC78)	XP_006720906.1:n.1054-59_1054-50del
XM_011522356.1:c.1501-59_1501-50del (CCDC78)	XP_011520658.1:n.1501-59_1501-50del
XM_011522357.1:c.1489-59_1489-50del (CCDC78)	XP_011520659.1:n.1489-59_1489-50del
XM_011522358.1:c.1501-59_1501-50del (CCDC78)	XP_011520660.1:n.1501-59_1501-50del
XM_011522359.1:c.1468-59_1468-50del (CCDC78)	XP_011520661.1:n.1468-59_1468-50del
XM_011522360.1:c.1456-59_1456-50del (CCDC78)	XP_011520662.1:n.1456-59_1456-50del
XM_011522361.1:c.1501-59_1501-50del (CCDC78)	XP_011520663.1:n.1501-59_1501-50del
XM_011522362.1:c.1501-59_1501-50del (CCDC78)	XP_011520664.1:n.1501-59_1501-50del
XM_011522363.1:c.1501-59_1501-50del (CCDC78)	XP_011520665.1:n.1501-59_1501-50del
XM_011522364.1:c.1501-59_1501-50del (CCDC78)	XP_011520666.1:n.1501-59_1501-50del
XM_011522365.1:c.1288-59_1288-50del (CCDC78)	XP_011520667.1:n.1288-59_1288-50del
XM_011522366.1:c.1279-59_1279-50del (CCDC78)	XP_011520668.1:n.1279-59_1279-50del
XM_011522367.1:c.1120-59_1120-50del (CCDC78)	XP_011520669.1:n.1120-59_1120-50del
XM_011522368.1:c.1108-59_1108-50del (CCDC78)	XP_011520670.1:n.1108-59_1108-50del
XM_011522369.1:c.1066-59_1066-50del (CCDC78)	XP_011520671.1:n.1066-59_1066-50del
XM_011522370.1:c.898-59_898-50del (CCDC78)	XP_011520672.1:n.898-59_898-50del
XM_011522371.1:c.613-59_613-50del (CCDC78)	XP_011520673.1:n.613-59_613-50del
XM_006720843.4:c.1054-59_1054-50del (CCDC78)	XP_006720906.1:n.1054-59_1054-50del
XM_011522358.2:c.1501-59_1501-50del (CCDC78)	XP_011520660.1:n.1501-59_1501-50del
XM_011522371.2:c.613-59_613-50del (CCDC78)	XP_011520673.1:n.613-59_613-50del
XM_017022929.1:c.1501-59_1501-50del (CCDC78)	XP_016878418.1:n.1501-59_1501-50del
XM_017022930.1:c.601-59_601-50del (CCDC78)	XP_016878419.1:n.601-59_601-50del
XM_017022931.1:c.-259_-250del (CCDC78)	XP_016878420.1:n.-259_-250del
XM_024450150.1:c.331-59_331-50del (CCDC78)	XP_024305918.1:n.331-59_331-50del
XR_001751835.1:n.1840-59_1840-50del (CCDC78)
XR_001751836.1:n.1819-59_1819-50del (CCDC78)
XR_001751837.1:n.1597-59_1597-50del (CCDC78)
XR_001751838.1:n.1943-59_1943-50del (CCDC78)
XR_001751839.1:n.1405-59_1405-50del (CCDC78)
NM_001031737.3:c.1054-59_1054-50del (CCDC78)	NP_001026907.2:n.1054-59_1054-50del
NM_001378030.1:c.1054-59_1054-50del (CCDC78) MANE Select	NP_001364959.1:n.1054-59_1054-50del
NM_001378031.1:c.953+327_953+336del (CCDC78)	NP_001364960.1:n.953+327_953+336del
NM_001378033.1:c.487-59_487-50del (CCDC78)	NP_001364962.1:n.487-59_487-50del
NR_165382.1:n.1611-59_1611-50del (CCDC78)
NR_165383.1:n.1257-59_1257-50del (CCDC78)
NR_165384.1:n.1222-59_1222-50del (CCDC78)
NR_165385.1:n.1322-59_1322-50del (CCDC78)
NR_165386.1:n.1389-59_1389-50del (CCDC78)