Canonical Allele Identifier: CA2575865226

Gene: CCDC78 MSLN

Linked Data

• dbSNP Id: rs2151550024

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724045_724062del , CM000678.2:g.724045_724062del	GRCh38
NC_000016.9:g.774045_774062del , CM000678.1:g.774045_774062del	GRCh37
NC_000016.8:g.714046_714063del	NCBI36
NG_032932.1:g.7415_7432del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1596+47_1596+64del (CCDC78)
ENST00000345165.10:c.1053+47_1053+64del (CCDC78) MANE Select	ENSP00000316851.5:n.1053+47_1053+64del
ENST00000293889.10:c.1053+47_1053+64del (CCDC78)	ENSP00000293889.6:n.1053+47_1053+64del
ENST00000345165.8:c.599+47_599+64del (CCDC78)
ENST00000463539.5:n.1375+47_1375+64del (CCDC78)
ENST00000466708.5:n.1397+47_1397+64del (CCDC78)
ENST00000478979.5:n.1578_1595del (CCDC78)
ENST00000481804.5:n.2031+47_2031+64del (CCDC78)
ENST00000482152.1:n.414+47_414+64del (CCDC78)
ENST00000482878.5:n.1981_1998del (CCDC78)
ENST00000485091.5:n.1206+47_1206+64del (CCDC78)
ENST00000620831.4:c.-49-38587_-49-38570del (MSLN)	ENSP00000482893.1:n.-49-38587_-49-38570del
NM_001031737.2:c.1053+47_1053+64del (CCDC78)	NP_001026907.2:n.1053+47_1053+64del
XM_006720838.1:c.1275+47_1275+64del (CCDC78)	XP_006720901.1:n.1275+47_1275+64del
XM_006720843.2:c.1053+47_1053+64del (CCDC78)	XP_006720906.1:n.1053+47_1053+64del
XM_011522356.1:c.1500+47_1500+64del (CCDC78)	XP_011520658.1:n.1500+47_1500+64del
XM_011522357.1:c.1488+47_1488+64del (CCDC78)	XP_011520659.1:n.1488+47_1488+64del
XM_011522358.1:c.1500+47_1500+64del (CCDC78)	XP_011520660.1:n.1500+47_1500+64del
XM_011522359.1:c.1467+47_1467+64del (CCDC78)	XP_011520661.1:n.1467+47_1467+64del
XM_011522360.1:c.1455+47_1455+64del (CCDC78)	XP_011520662.1:n.1455+47_1455+64del
XM_011522361.1:c.1500+47_1500+64del (CCDC78)	XP_011520663.1:n.1500+47_1500+64del
XM_011522362.1:c.1500+47_1500+64del (CCDC78)	XP_011520664.1:n.1500+47_1500+64del
XM_011522363.1:c.1500+47_1500+64del (CCDC78)	XP_011520665.1:n.1500+47_1500+64del
XM_011522364.1:c.1500+47_1500+64del (CCDC78)	XP_011520666.1:n.1500+47_1500+64del
XM_011522365.1:c.1287+47_1287+64del (CCDC78)	XP_011520667.1:n.1287+47_1287+64del
XM_011522366.1:c.1278+47_1278+64del (CCDC78)	XP_011520668.1:n.1278+47_1278+64del
XM_011522367.1:c.1119+47_1119+64del (CCDC78)	XP_011520669.1:n.1119+47_1119+64del
XM_011522368.1:c.1107+47_1107+64del (CCDC78)	XP_011520670.1:n.1107+47_1107+64del
XM_011522369.1:c.1065+47_1065+64del (CCDC78)	XP_011520671.1:n.1065+47_1065+64del
XM_011522370.1:c.897+47_897+64del (CCDC78)	XP_011520672.1:n.897+47_897+64del
XM_011522371.1:c.612+47_612+64del (CCDC78)	XP_011520673.1:n.612+47_612+64del
XM_006720843.4:c.1053+47_1053+64del (CCDC78)	XP_006720906.1:n.1053+47_1053+64del
XM_011522358.2:c.1500+47_1500+64del (CCDC78)	XP_011520660.1:n.1500+47_1500+64del
XM_011522371.2:c.612+47_612+64del (CCDC78)	XP_011520673.1:n.612+47_612+64del
XM_017022929.1:c.1500+47_1500+64del (CCDC78)	XP_016878418.1:n.1500+47_1500+64del
XM_017022930.1:c.600+47_600+64del (CCDC78)	XP_016878419.1:n.600+47_600+64del
XM_017022931.1:c.-323_-306del (CCDC78)	XP_016878420.1:n.-323_-306del
XM_024450150.1:c.330+47_330+64del (CCDC78)	XP_024305918.1:n.330+47_330+64del
XR_001751835.1:n.1839+47_1839+64del (CCDC78)
XR_001751836.1:n.1818+47_1818+64del (CCDC78)
XR_001751837.1:n.1596+47_1596+64del (CCDC78)
XR_001751838.1:n.1942+47_1942+64del (CCDC78)
XR_001751839.1:n.1404+47_1404+64del (CCDC78)
NM_001031737.3:c.1053+47_1053+64del (CCDC78)	NP_001026907.2:n.1053+47_1053+64del
NM_001378030.1:c.1053+47_1053+64del (CCDC78) MANE Select	NP_001364959.1:n.1053+47_1053+64del
NM_001378031.1:c.953+263_953+280del (CCDC78)	NP_001364960.1:n.953+263_953+280del
NM_001378033.1:c.486+47_486+64del (CCDC78)	NP_001364962.1:n.486+47_486+64del
NR_165382.1:n.1610+47_1610+64del (CCDC78)
NR_165383.1:n.1256+47_1256+64del (CCDC78)
NR_165384.1:n.1221+47_1221+64del (CCDC78)
NR_165385.1:n.1321+47_1321+64del (CCDC78)
NR_165386.1:n.1388+47_1388+64del (CCDC78)