Canonical Allele Identifier: CA276519652

Gene: CCDC78 MSLN

Linked Data

• dbSNP Id: rs898666209
• gnomAD v3: 16-723721-G-A
• gnomAD v4: 16-723721-G-A
• MyVariant Identifiers: chr16:g.723721G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723721G>A , CM000678.2:g.723721G>A	GRCh38
NC_000016.9:g.773721G>A , CM000678.1:g.773721G>A	GRCh37
NC_000016.8:g.713722G>A	NCBI36
NG_032932.1:g.7753C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1676+136C>T (CCDC78)
ENST00000345165.10:c.1133+136C>T (CCDC78) MANE Select	ENSP00000316851.5:n.1133+136C>T
ENST00000293889.10:c.1133+136C>T (CCDC78)	ENSP00000293889.6:n.1133+136C>T
ENST00000345165.8:c.679+136C>T (CCDC78)
ENST00000463539.5:n.1455+136C>T (CCDC78)
ENST00000466708.5:n.1477+136C>T (CCDC78)
ENST00000478979.5:n.1916C>T (CCDC78)
ENST00000481804.5:n.2247C>T (CCDC78)
ENST00000482152.1:n.494+136C>T (CCDC78)
ENST00000482878.5:n.2319C>T (CCDC78)
ENST00000485091.5:n.1286+136C>T (CCDC78)
ENST00000620831.4:c.-49-38911G>A (MSLN)	ENSP00000482893.1:n.-49-38911G>A
NM_001031737.2:c.1133+136C>T (CCDC78)	NP_001026907.2:n.1133+136C>T
XM_006720838.1:c.1355+136C>T (CCDC78)	XP_006720901.1:n.1355+136C>T
XM_006720843.2:c.1133+136C>T (CCDC78)	XP_006720906.1:n.1133+136C>T
XM_011522356.1:c.1580+136C>T (CCDC78)	XP_011520658.1:n.1580+136C>T
XM_011522357.1:c.1568+136C>T (CCDC78)	XP_011520659.1:n.1568+136C>T
XM_011522358.1:c.1580+136C>T (CCDC78)	XP_011520660.1:n.1580+136C>T
XM_011522359.1:c.1547+136C>T (CCDC78)	XP_011520661.1:n.1547+136C>T
XM_011522360.1:c.1535+136C>T (CCDC78)	XP_011520662.1:n.1535+136C>T
XM_011522361.1:c.1580+136C>T (CCDC78)	XP_011520663.1:n.1580+136C>T
XM_011522362.1:c.1580+136C>T (CCDC78)	XP_011520664.1:n.1580+136C>T
XM_011522363.1:c.1580+136C>T (CCDC78)	XP_011520665.1:n.1580+136C>T
XM_011522364.1:c.1580+136C>T (CCDC78)	XP_011520666.1:n.1580+136C>T
XM_011522365.1:c.1367+136C>T (CCDC78)	XP_011520667.1:n.1367+136C>T
XM_011522366.1:c.1358+136C>T (CCDC78)	XP_011520668.1:n.1358+136C>T
XM_011522367.1:c.1199+136C>T (CCDC78)	XP_011520669.1:n.1199+136C>T
XM_011522368.1:c.1187+136C>T (CCDC78)	XP_011520670.1:n.1187+136C>T
XM_011522369.1:c.1145+136C>T (CCDC78)	XP_011520671.1:n.1145+136C>T
XM_011522370.1:c.977+136C>T (CCDC78)	XP_011520672.1:n.977+136C>T
XM_011522371.1:c.692+136C>T (CCDC78)	XP_011520673.1:n.692+136C>T
XM_006720843.4:c.1133+136C>T (CCDC78)	XP_006720906.1:n.1133+136C>T
XM_011522358.2:c.1580+136C>T (CCDC78)	XP_011520660.1:n.1580+136C>T
XM_011522371.2:c.692+136C>T (CCDC78)	XP_011520673.1:n.692+136C>T
XM_017022929.1:c.1580+136C>T (CCDC78)	XP_016878418.1:n.1580+136C>T
XM_017022930.1:c.680+136C>T (CCDC78)	XP_016878419.1:n.680+136C>T
XM_017022931.1:c.16C>T (CCDC78)	XP_016878420.1:p.His6Tyr
XM_024450150.1:c.410+136C>T (CCDC78)	XP_024305918.1:n.410+136C>T
XR_001751835.1:n.1919+136C>T (CCDC78)
XR_001751836.1:n.1898+136C>T (CCDC78)
XR_001751837.1:n.1676+136C>T (CCDC78)
XR_001751838.1:n.2022+136C>T (CCDC78)
XR_001751839.1:n.1484+136C>T (CCDC78)
NM_001031737.3:c.1133+136C>T (CCDC78)	NP_001026907.2:n.1133+136C>T
NM_001378030.1:c.1133+136C>T (CCDC78) MANE Select	NP_001364959.1:n.1133+136C>T
NM_001378031.1:c.954-560C>T (CCDC78)	NP_001364960.1:n.954-560C>T
NM_001378033.1:c.566+136C>T (CCDC78)	NP_001364962.1:n.566+136C>T
NR_165382.1:n.1690+136C>T (CCDC78)
NR_165383.1:n.1336+136C>T (CCDC78)
NR_165384.1:n.1301+136C>T (CCDC78)
NR_165385.1:n.1401+136C>T (CCDC78)
NR_165386.1:n.1468+136C>T (CCDC78)