Canonical Allele Identifier: CA2630857763

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-724050-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724051_724052del , CM000678.2:g.724051_724052del	GRCh38
NC_000016.9:g.774051_774052del , CM000678.1:g.774051_774052del	GRCh37
NC_000016.8:g.714052_714053del	NCBI36
NG_032932.1:g.7422_7423del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1596+54_1596+55del (CCDC78)
ENST00000345165.10:c.1053+54_1053+55del (CCDC78) MANE Select	ENSP00000316851.5:n.1053+54_1053+55del
ENST00000293889.10:c.1053+54_1053+55del (CCDC78)	ENSP00000293889.6:n.1053+54_1053+55del
ENST00000345165.8:c.599+54_599+55del (CCDC78)
ENST00000463539.5:n.1375+54_1375+55del (CCDC78)
ENST00000466708.5:n.1397+54_1397+55del (CCDC78)
ENST00000478979.5:n.1585_1586del (CCDC78)
ENST00000481804.5:n.2031+54_2031+55del (CCDC78)
ENST00000482152.1:n.414+54_414+55del (CCDC78)
ENST00000482878.5:n.1988_1989del (CCDC78)
ENST00000485091.5:n.1206+54_1206+55del (CCDC78)
ENST00000620831.4:c.-49-38581_-49-38580del (MSLN)	ENSP00000482893.1:n.-49-38581_-49-38580del
NM_001031737.2:c.1053+54_1053+55del (CCDC78)	NP_001026907.2:n.1053+54_1053+55del
XM_006720838.1:c.1275+54_1275+55del (CCDC78)	XP_006720901.1:n.1275+54_1275+55del
XM_006720843.2:c.1053+54_1053+55del (CCDC78)	XP_006720906.1:n.1053+54_1053+55del
XM_011522356.1:c.1500+54_1500+55del (CCDC78)	XP_011520658.1:n.1500+54_1500+55del
XM_011522357.1:c.1488+54_1488+55del (CCDC78)	XP_011520659.1:n.1488+54_1488+55del
XM_011522358.1:c.1500+54_1500+55del (CCDC78)	XP_011520660.1:n.1500+54_1500+55del
XM_011522359.1:c.1467+54_1467+55del (CCDC78)	XP_011520661.1:n.1467+54_1467+55del
XM_011522360.1:c.1455+54_1455+55del (CCDC78)	XP_011520662.1:n.1455+54_1455+55del
XM_011522361.1:c.1500+54_1500+55del (CCDC78)	XP_011520663.1:n.1500+54_1500+55del
XM_011522362.1:c.1500+54_1500+55del (CCDC78)	XP_011520664.1:n.1500+54_1500+55del
XM_011522363.1:c.1500+54_1500+55del (CCDC78)	XP_011520665.1:n.1500+54_1500+55del
XM_011522364.1:c.1500+54_1500+55del (CCDC78)	XP_011520666.1:n.1500+54_1500+55del
XM_011522365.1:c.1287+54_1287+55del (CCDC78)	XP_011520667.1:n.1287+54_1287+55del
XM_011522366.1:c.1278+54_1278+55del (CCDC78)	XP_011520668.1:n.1278+54_1278+55del
XM_011522367.1:c.1119+54_1119+55del (CCDC78)	XP_011520669.1:n.1119+54_1119+55del
XM_011522368.1:c.1107+54_1107+55del (CCDC78)	XP_011520670.1:n.1107+54_1107+55del
XM_011522369.1:c.1065+54_1065+55del (CCDC78)	XP_011520671.1:n.1065+54_1065+55del
XM_011522370.1:c.897+54_897+55del (CCDC78)	XP_011520672.1:n.897+54_897+55del
XM_011522371.1:c.612+54_612+55del (CCDC78)	XP_011520673.1:n.612+54_612+55del
XM_006720843.4:c.1053+54_1053+55del (CCDC78)	XP_006720906.1:n.1053+54_1053+55del
XM_011522358.2:c.1500+54_1500+55del (CCDC78)	XP_011520660.1:n.1500+54_1500+55del
XM_011522371.2:c.612+54_612+55del (CCDC78)	XP_011520673.1:n.612+54_612+55del
XM_017022929.1:c.1500+54_1500+55del (CCDC78)	XP_016878418.1:n.1500+54_1500+55del
XM_017022930.1:c.600+54_600+55del (CCDC78)	XP_016878419.1:n.600+54_600+55del
XM_017022931.1:c.-316_-315del (CCDC78)	XP_016878420.1:n.-316_-315del
XM_024450150.1:c.330+54_330+55del (CCDC78)	XP_024305918.1:n.330+54_330+55del
XR_001751835.1:n.1839+54_1839+55del (CCDC78)
XR_001751836.1:n.1818+54_1818+55del (CCDC78)
XR_001751837.1:n.1596+54_1596+55del (CCDC78)
XR_001751838.1:n.1942+54_1942+55del (CCDC78)
XR_001751839.1:n.1404+54_1404+55del (CCDC78)
NM_001031737.3:c.1053+54_1053+55del (CCDC78)	NP_001026907.2:n.1053+54_1053+55del
NM_001378030.1:c.1053+54_1053+55del (CCDC78) MANE Select	NP_001364959.1:n.1053+54_1053+55del
NM_001378031.1:c.953+270_953+271del (CCDC78)	NP_001364960.1:n.953+270_953+271del
NM_001378033.1:c.486+54_486+55del (CCDC78)	NP_001364962.1:n.486+54_486+55del
NR_165382.1:n.1610+54_1610+55del (CCDC78)
NR_165383.1:n.1256+54_1256+55del (CCDC78)
NR_165384.1:n.1221+54_1221+55del (CCDC78)
NR_165385.1:n.1321+54_1321+55del (CCDC78)
NR_165386.1:n.1388+54_1388+55del (CCDC78)