Canonical Allele Identifier: CA2805525147

Gene: CCDC78 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723998_723999insT , CM000678.2:g.723998_723999insT	GRCh38
NC_000016.9:g.773998_773999insT , CM000678.1:g.773998_773999insT	GRCh37
NC_000016.8:g.713999_714000insT	NCBI36
NG_032932.1:g.7475_7476insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1597-63_1597-62insA (CCDC78)
ENST00000345165.10:c.1054-63_1054-62insA (CCDC78) MANE Select	ENSP00000316851.5:n.1054-63_1054-62insA
ENST00000293889.10:c.1054-63_1054-62insA (CCDC78)	ENSP00000293889.6:n.1054-63_1054-62insA
ENST00000345165.8:c.600-63_600-62insA (CCDC78)
ENST00000463539.5:n.1376-63_1376-62insA (CCDC78)
ENST00000466708.5:n.1398-63_1398-62insA (CCDC78)
ENST00000478979.5:n.1638_1639insA (CCDC78)
ENST00000481804.5:n.2032-63_2032-62insA (CCDC78)
ENST00000482152.1:n.415-63_415-62insA (CCDC78)
ENST00000482878.5:n.2041_2042insA (CCDC78)
ENST00000485091.5:n.1207-63_1207-62insA (CCDC78)
ENST00000620831.4:c.-49-38634_-49-38633insT (MSLN)	ENSP00000482893.1:n.-49-38634_-49-38633insT
NM_001031737.2:c.1054-63_1054-62insA (CCDC78)	NP_001026907.2:n.1054-63_1054-62insA
XM_006720838.1:c.1276-63_1276-62insA (CCDC78)	XP_006720901.1:n.1276-63_1276-62insA
XM_006720843.2:c.1054-63_1054-62insA (CCDC78)	XP_006720906.1:n.1054-63_1054-62insA
XM_011522356.1:c.1501-63_1501-62insA (CCDC78)	XP_011520658.1:n.1501-63_1501-62insA
XM_011522357.1:c.1489-63_1489-62insA (CCDC78)	XP_011520659.1:n.1489-63_1489-62insA
XM_011522358.1:c.1501-63_1501-62insA (CCDC78)	XP_011520660.1:n.1501-63_1501-62insA
XM_011522359.1:c.1468-63_1468-62insA (CCDC78)	XP_011520661.1:n.1468-63_1468-62insA
XM_011522360.1:c.1456-63_1456-62insA (CCDC78)	XP_011520662.1:n.1456-63_1456-62insA
XM_011522361.1:c.1501-63_1501-62insA (CCDC78)	XP_011520663.1:n.1501-63_1501-62insA
XM_011522362.1:c.1501-63_1501-62insA (CCDC78)	XP_011520664.1:n.1501-63_1501-62insA
XM_011522363.1:c.1501-63_1501-62insA (CCDC78)	XP_011520665.1:n.1501-63_1501-62insA
XM_011522364.1:c.1501-63_1501-62insA (CCDC78)	XP_011520666.1:n.1501-63_1501-62insA
XM_011522365.1:c.1288-63_1288-62insA (CCDC78)	XP_011520667.1:n.1288-63_1288-62insA
XM_011522366.1:c.1279-63_1279-62insA (CCDC78)	XP_011520668.1:n.1279-63_1279-62insA
XM_011522367.1:c.1120-63_1120-62insA (CCDC78)	XP_011520669.1:n.1120-63_1120-62insA
XM_011522368.1:c.1108-63_1108-62insA (CCDC78)	XP_011520670.1:n.1108-63_1108-62insA
XM_011522369.1:c.1066-63_1066-62insA (CCDC78)	XP_011520671.1:n.1066-63_1066-62insA
XM_011522370.1:c.898-63_898-62insA (CCDC78)	XP_011520672.1:n.898-63_898-62insA
XM_011522371.1:c.613-63_613-62insA (CCDC78)	XP_011520673.1:n.613-63_613-62insA
XM_006720843.4:c.1054-63_1054-62insA (CCDC78)	XP_006720906.1:n.1054-63_1054-62insA
XM_011522358.2:c.1501-63_1501-62insA (CCDC78)	XP_011520660.1:n.1501-63_1501-62insA
XM_011522371.2:c.613-63_613-62insA (CCDC78)	XP_011520673.1:n.613-63_613-62insA
XM_017022929.1:c.1501-63_1501-62insA (CCDC78)	XP_016878418.1:n.1501-63_1501-62insA
XM_017022930.1:c.601-63_601-62insA (CCDC78)	XP_016878419.1:n.601-63_601-62insA
XM_017022931.1:c.-263_-262insA (CCDC78)	XP_016878420.1:n.-263_-262insA
XM_024450150.1:c.331-63_331-62insA (CCDC78)	XP_024305918.1:n.331-63_331-62insA
XR_001751835.1:n.1840-63_1840-62insA (CCDC78)
XR_001751836.1:n.1819-63_1819-62insA (CCDC78)
XR_001751837.1:n.1597-63_1597-62insA (CCDC78)
XR_001751838.1:n.1943-63_1943-62insA (CCDC78)
XR_001751839.1:n.1405-63_1405-62insA (CCDC78)
NM_001031737.3:c.1054-63_1054-62insA (CCDC78)	NP_001026907.2:n.1054-63_1054-62insA
NM_001378030.1:c.1054-63_1054-62insA (CCDC78) MANE Select	NP_001364959.1:n.1054-63_1054-62insA
NM_001378031.1:c.953+323_953+324insA (CCDC78)	NP_001364960.1:n.953+323_953+324insA
NM_001378033.1:c.487-63_487-62insA (CCDC78)	NP_001364962.1:n.487-63_487-62insA
NR_165382.1:n.1611-63_1611-62insA (CCDC78)
NR_165383.1:n.1257-63_1257-62insA (CCDC78)
NR_165384.1:n.1222-63_1222-62insA (CCDC78)
NR_165385.1:n.1322-63_1322-62insA (CCDC78)
NR_165386.1:n.1389-63_1389-62insA (CCDC78)