Canonical Allele Identifier: CA2630857258

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-724025-GATGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724026_724029del , CM000678.2:g.724026_724029del	GRCh38
NC_000016.9:g.774026_774029del , CM000678.1:g.774026_774029del	GRCh37
NC_000016.8:g.714027_714030del	NCBI36
NG_032932.1:g.7445_7448del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1596+77_1596+80del (CCDC78)
ENST00000345165.10:c.1053+77_1053+80del (CCDC78) MANE Select	ENSP00000316851.5:n.1053+77_1053+80del
ENST00000293889.10:c.1053+77_1053+80del (CCDC78)	ENSP00000293889.6:n.1053+77_1053+80del
ENST00000345165.8:c.599+77_599+80del (CCDC78)
ENST00000463539.5:n.1375+77_1375+80del (CCDC78)
ENST00000466708.5:n.1397+77_1397+80del (CCDC78)
ENST00000478979.5:n.1608_1611del (CCDC78)
ENST00000481804.5:n.2031+77_2031+80del (CCDC78)
ENST00000482152.1:n.414+77_414+80del (CCDC78)
ENST00000482878.5:n.2011_2014del (CCDC78)
ENST00000485091.5:n.1206+77_1206+80del (CCDC78)
ENST00000620831.4:c.-49-38606_-49-38603del (MSLN)	ENSP00000482893.1:n.-49-38606_-49-38603del
NM_001031737.2:c.1053+77_1053+80del (CCDC78)	NP_001026907.2:n.1053+77_1053+80del
XM_006720838.1:c.1275+77_1275+80del (CCDC78)	XP_006720901.1:n.1275+77_1275+80del
XM_006720843.2:c.1053+77_1053+80del (CCDC78)	XP_006720906.1:n.1053+77_1053+80del
XM_011522356.1:c.1500+77_1500+80del (CCDC78)	XP_011520658.1:n.1500+77_1500+80del
XM_011522357.1:c.1488+77_1488+80del (CCDC78)	XP_011520659.1:n.1488+77_1488+80del
XM_011522358.1:c.1500+77_1500+80del (CCDC78)	XP_011520660.1:n.1500+77_1500+80del
XM_011522359.1:c.1467+77_1467+80del (CCDC78)	XP_011520661.1:n.1467+77_1467+80del
XM_011522360.1:c.1455+77_1455+80del (CCDC78)	XP_011520662.1:n.1455+77_1455+80del
XM_011522361.1:c.1500+77_1500+80del (CCDC78)	XP_011520663.1:n.1500+77_1500+80del
XM_011522362.1:c.1500+77_1500+80del (CCDC78)	XP_011520664.1:n.1500+77_1500+80del
XM_011522363.1:c.1500+77_1500+80del (CCDC78)	XP_011520665.1:n.1500+77_1500+80del
XM_011522364.1:c.1500+77_1500+80del (CCDC78)	XP_011520666.1:n.1500+77_1500+80del
XM_011522365.1:c.1287+77_1287+80del (CCDC78)	XP_011520667.1:n.1287+77_1287+80del
XM_011522366.1:c.1278+77_1278+80del (CCDC78)	XP_011520668.1:n.1278+77_1278+80del
XM_011522367.1:c.1119+77_1119+80del (CCDC78)	XP_011520669.1:n.1119+77_1119+80del
XM_011522368.1:c.1107+77_1107+80del (CCDC78)	XP_011520670.1:n.1107+77_1107+80del
XM_011522369.1:c.1065+77_1065+80del (CCDC78)	XP_011520671.1:n.1065+77_1065+80del
XM_011522370.1:c.897+77_897+80del (CCDC78)	XP_011520672.1:n.897+77_897+80del
XM_011522371.1:c.612+77_612+80del (CCDC78)	XP_011520673.1:n.612+77_612+80del
XM_006720843.4:c.1053+77_1053+80del (CCDC78)	XP_006720906.1:n.1053+77_1053+80del
XM_011522358.2:c.1500+77_1500+80del (CCDC78)	XP_011520660.1:n.1500+77_1500+80del
XM_011522371.2:c.612+77_612+80del (CCDC78)	XP_011520673.1:n.612+77_612+80del
XM_017022929.1:c.1500+77_1500+80del (CCDC78)	XP_016878418.1:n.1500+77_1500+80del
XM_017022930.1:c.600+77_600+80del (CCDC78)	XP_016878419.1:n.600+77_600+80del
XM_017022931.1:c.-293_-290del (CCDC78)	XP_016878420.1:n.-293_-290del
XM_024450150.1:c.330+77_330+80del (CCDC78)	XP_024305918.1:n.330+77_330+80del
XR_001751835.1:n.1839+77_1839+80del (CCDC78)
XR_001751836.1:n.1818+77_1818+80del (CCDC78)
XR_001751837.1:n.1596+77_1596+80del (CCDC78)
XR_001751838.1:n.1942+77_1942+80del (CCDC78)
XR_001751839.1:n.1404+77_1404+80del (CCDC78)
NM_001031737.3:c.1053+77_1053+80del (CCDC78)	NP_001026907.2:n.1053+77_1053+80del
NM_001378030.1:c.1053+77_1053+80del (CCDC78) MANE Select	NP_001364959.1:n.1053+77_1053+80del
NM_001378031.1:c.953+293_953+296del (CCDC78)	NP_001364960.1:n.953+293_953+296del
NM_001378033.1:c.486+77_486+80del (CCDC78)	NP_001364962.1:n.486+77_486+80del
NR_165382.1:n.1610+77_1610+80del (CCDC78)
NR_165383.1:n.1256+77_1256+80del (CCDC78)
NR_165384.1:n.1221+77_1221+80del (CCDC78)
NR_165385.1:n.1321+77_1321+80del (CCDC78)
NR_165386.1:n.1388+77_1388+80del (CCDC78)