Canonical Allele Identifier: CA2630857801

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-724053-T-TGG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724055_724056dup , CM000678.2:g.724055_724056dup	GRCh38
NC_000016.9:g.774055_774056dup , CM000678.1:g.774055_774056dup	GRCh37
NC_000016.8:g.714056_714057dup	NCBI36
NG_032932.1:g.7419_7420dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1596+51_1596+52dup (CCDC78)
ENST00000345165.10:c.1053+51_1053+52dup (CCDC78) MANE Select	ENSP00000316851.5:n.1053+51_1053+52dup
ENST00000293889.10:c.1053+51_1053+52dup (CCDC78)	ENSP00000293889.6:n.1053+51_1053+52dup
ENST00000345165.8:c.599+51_599+52dup (CCDC78)
ENST00000463539.5:n.1375+51_1375+52dup (CCDC78)
ENST00000466708.5:n.1397+51_1397+52dup (CCDC78)
ENST00000478979.5:n.1582_1583dup (CCDC78)
ENST00000481804.5:n.2031+51_2031+52dup (CCDC78)
ENST00000482152.1:n.414+51_414+52dup (CCDC78)
ENST00000482878.5:n.1985_1986dup (CCDC78)
ENST00000485091.5:n.1206+51_1206+52dup (CCDC78)
ENST00000620831.4:c.-49-38577_-49-38576dup (MSLN)	ENSP00000482893.1:n.-49-38577_-49-38576dup
NM_001031737.2:c.1053+51_1053+52dup (CCDC78)	NP_001026907.2:n.1053+51_1053+52dup
XM_006720838.1:c.1275+51_1275+52dup (CCDC78)	XP_006720901.1:n.1275+51_1275+52dup
XM_006720843.2:c.1053+51_1053+52dup (CCDC78)	XP_006720906.1:n.1053+51_1053+52dup
XM_011522356.1:c.1500+51_1500+52dup (CCDC78)	XP_011520658.1:n.1500+51_1500+52dup
XM_011522357.1:c.1488+51_1488+52dup (CCDC78)	XP_011520659.1:n.1488+51_1488+52dup
XM_011522358.1:c.1500+51_1500+52dup (CCDC78)	XP_011520660.1:n.1500+51_1500+52dup
XM_011522359.1:c.1467+51_1467+52dup (CCDC78)	XP_011520661.1:n.1467+51_1467+52dup
XM_011522360.1:c.1455+51_1455+52dup (CCDC78)	XP_011520662.1:n.1455+51_1455+52dup
XM_011522361.1:c.1500+51_1500+52dup (CCDC78)	XP_011520663.1:n.1500+51_1500+52dup
XM_011522362.1:c.1500+51_1500+52dup (CCDC78)	XP_011520664.1:n.1500+51_1500+52dup
XM_011522363.1:c.1500+51_1500+52dup (CCDC78)	XP_011520665.1:n.1500+51_1500+52dup
XM_011522364.1:c.1500+51_1500+52dup (CCDC78)	XP_011520666.1:n.1500+51_1500+52dup
XM_011522365.1:c.1287+51_1287+52dup (CCDC78)	XP_011520667.1:n.1287+51_1287+52dup
XM_011522366.1:c.1278+51_1278+52dup (CCDC78)	XP_011520668.1:n.1278+51_1278+52dup
XM_011522367.1:c.1119+51_1119+52dup (CCDC78)	XP_011520669.1:n.1119+51_1119+52dup
XM_011522368.1:c.1107+51_1107+52dup (CCDC78)	XP_011520670.1:n.1107+51_1107+52dup
XM_011522369.1:c.1065+51_1065+52dup (CCDC78)	XP_011520671.1:n.1065+51_1065+52dup
XM_011522370.1:c.897+51_897+52dup (CCDC78)	XP_011520672.1:n.897+51_897+52dup
XM_011522371.1:c.612+51_612+52dup (CCDC78)	XP_011520673.1:n.612+51_612+52dup
XM_006720843.4:c.1053+51_1053+52dup (CCDC78)	XP_006720906.1:n.1053+51_1053+52dup
XM_011522358.2:c.1500+51_1500+52dup (CCDC78)	XP_011520660.1:n.1500+51_1500+52dup
XM_011522371.2:c.612+51_612+52dup (CCDC78)	XP_011520673.1:n.612+51_612+52dup
XM_017022929.1:c.1500+51_1500+52dup (CCDC78)	XP_016878418.1:n.1500+51_1500+52dup
XM_017022930.1:c.600+51_600+52dup (CCDC78)	XP_016878419.1:n.600+51_600+52dup
XM_017022931.1:c.-319_-318dup (CCDC78)	XP_016878420.1:n.-319_-318dup
XM_024450150.1:c.330+51_330+52dup (CCDC78)	XP_024305918.1:n.330+51_330+52dup
XR_001751835.1:n.1839+51_1839+52dup (CCDC78)
XR_001751836.1:n.1818+51_1818+52dup (CCDC78)
XR_001751837.1:n.1596+51_1596+52dup (CCDC78)
XR_001751838.1:n.1942+51_1942+52dup (CCDC78)
XR_001751839.1:n.1404+51_1404+52dup (CCDC78)
NM_001031737.3:c.1053+51_1053+52dup (CCDC78)	NP_001026907.2:n.1053+51_1053+52dup
NM_001378030.1:c.1053+51_1053+52dup (CCDC78) MANE Select	NP_001364959.1:n.1053+51_1053+52dup
NM_001378031.1:c.953+267_953+268dup (CCDC78)	NP_001364960.1:n.953+267_953+268dup
NM_001378033.1:c.486+51_486+52dup (CCDC78)	NP_001364962.1:n.486+51_486+52dup
NR_165382.1:n.1610+51_1610+52dup (CCDC78)
NR_165383.1:n.1256+51_1256+52dup (CCDC78)
NR_165384.1:n.1221+51_1221+52dup (CCDC78)
NR_165385.1:n.1321+51_1321+52dup (CCDC78)
NR_165386.1:n.1388+51_1388+52dup (CCDC78)