Canonical Allele Identifier: CA2630857761

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-724050-CAGTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724051_724054del , CM000678.2:g.724051_724054del	GRCh38
NC_000016.9:g.774051_774054del , CM000678.1:g.774051_774054del	GRCh37
NC_000016.8:g.714052_714055del	NCBI36
NG_032932.1:g.7420_7423del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1596+52_1596+55del (CCDC78)
ENST00000345165.10:c.1053+52_1053+55del (CCDC78) MANE Select	ENSP00000316851.5:n.1053+52_1053+55del
ENST00000293889.10:c.1053+52_1053+55del (CCDC78)	ENSP00000293889.6:n.1053+52_1053+55del
ENST00000345165.8:c.599+52_599+55del (CCDC78)
ENST00000463539.5:n.1375+52_1375+55del (CCDC78)
ENST00000466708.5:n.1397+52_1397+55del (CCDC78)
ENST00000478979.5:n.1583_1586del (CCDC78)
ENST00000481804.5:n.2031+52_2031+55del (CCDC78)
ENST00000482152.1:n.414+52_414+55del (CCDC78)
ENST00000482878.5:n.1986_1989del (CCDC78)
ENST00000485091.5:n.1206+52_1206+55del (CCDC78)
ENST00000620831.4:c.-49-38581_-49-38578del (MSLN)	ENSP00000482893.1:n.-49-38581_-49-38578del
NM_001031737.2:c.1053+52_1053+55del (CCDC78)	NP_001026907.2:n.1053+52_1053+55del
XM_006720838.1:c.1275+52_1275+55del (CCDC78)	XP_006720901.1:n.1275+52_1275+55del
XM_006720843.2:c.1053+52_1053+55del (CCDC78)	XP_006720906.1:n.1053+52_1053+55del
XM_011522356.1:c.1500+52_1500+55del (CCDC78)	XP_011520658.1:n.1500+52_1500+55del
XM_011522357.1:c.1488+52_1488+55del (CCDC78)	XP_011520659.1:n.1488+52_1488+55del
XM_011522358.1:c.1500+52_1500+55del (CCDC78)	XP_011520660.1:n.1500+52_1500+55del
XM_011522359.1:c.1467+52_1467+55del (CCDC78)	XP_011520661.1:n.1467+52_1467+55del
XM_011522360.1:c.1455+52_1455+55del (CCDC78)	XP_011520662.1:n.1455+52_1455+55del
XM_011522361.1:c.1500+52_1500+55del (CCDC78)	XP_011520663.1:n.1500+52_1500+55del
XM_011522362.1:c.1500+52_1500+55del (CCDC78)	XP_011520664.1:n.1500+52_1500+55del
XM_011522363.1:c.1500+52_1500+55del (CCDC78)	XP_011520665.1:n.1500+52_1500+55del
XM_011522364.1:c.1500+52_1500+55del (CCDC78)	XP_011520666.1:n.1500+52_1500+55del
XM_011522365.1:c.1287+52_1287+55del (CCDC78)	XP_011520667.1:n.1287+52_1287+55del
XM_011522366.1:c.1278+52_1278+55del (CCDC78)	XP_011520668.1:n.1278+52_1278+55del
XM_011522367.1:c.1119+52_1119+55del (CCDC78)	XP_011520669.1:n.1119+52_1119+55del
XM_011522368.1:c.1107+52_1107+55del (CCDC78)	XP_011520670.1:n.1107+52_1107+55del
XM_011522369.1:c.1065+52_1065+55del (CCDC78)	XP_011520671.1:n.1065+52_1065+55del
XM_011522370.1:c.897+52_897+55del (CCDC78)	XP_011520672.1:n.897+52_897+55del
XM_011522371.1:c.612+52_612+55del (CCDC78)	XP_011520673.1:n.612+52_612+55del
XM_006720843.4:c.1053+52_1053+55del (CCDC78)	XP_006720906.1:n.1053+52_1053+55del
XM_011522358.2:c.1500+52_1500+55del (CCDC78)	XP_011520660.1:n.1500+52_1500+55del
XM_011522371.2:c.612+52_612+55del (CCDC78)	XP_011520673.1:n.612+52_612+55del
XM_017022929.1:c.1500+52_1500+55del (CCDC78)	XP_016878418.1:n.1500+52_1500+55del
XM_017022930.1:c.600+52_600+55del (CCDC78)	XP_016878419.1:n.600+52_600+55del
XM_017022931.1:c.-318_-315del (CCDC78)	XP_016878420.1:n.-318_-315del
XM_024450150.1:c.330+52_330+55del (CCDC78)	XP_024305918.1:n.330+52_330+55del
XR_001751835.1:n.1839+52_1839+55del (CCDC78)
XR_001751836.1:n.1818+52_1818+55del (CCDC78)
XR_001751837.1:n.1596+52_1596+55del (CCDC78)
XR_001751838.1:n.1942+52_1942+55del (CCDC78)
XR_001751839.1:n.1404+52_1404+55del (CCDC78)
NM_001031737.3:c.1053+52_1053+55del (CCDC78)	NP_001026907.2:n.1053+52_1053+55del
NM_001378030.1:c.1053+52_1053+55del (CCDC78) MANE Select	NP_001364959.1:n.1053+52_1053+55del
NM_001378031.1:c.953+268_953+271del (CCDC78)	NP_001364960.1:n.953+268_953+271del
NM_001378033.1:c.486+52_486+55del (CCDC78)	NP_001364962.1:n.486+52_486+55del
NR_165382.1:n.1610+52_1610+55del (CCDC78)
NR_165383.1:n.1256+52_1256+55del (CCDC78)
NR_165384.1:n.1221+52_1221+55del (CCDC78)
NR_165385.1:n.1321+52_1321+55del (CCDC78)
NR_165386.1:n.1388+52_1388+55del (CCDC78)