Canonical Allele Identifier: CA394098844

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.774132T>A (hg19) ; chr16:g.724132T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724132T>A , CM000678.2:g.724132T>A	GRCh38
NC_000016.9:g.774132T>A , CM000678.1:g.774132T>A	GRCh37
NC_000016.8:g.714133T>A	NCBI36
NG_032932.1:g.7342A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1570A>T (CCDC78)
ENST00000345165.10:c.1027A>T (CCDC78) MANE Select	ENSP00000316851.5:p.Thr343Ser
ENST00000293889.10:c.1027A>T (CCDC78)	ENSP00000293889.6:p.Thr343Ser
ENST00000345165.8:c.573A>T (CCDC78)
ENST00000463539.5:n.1349A>T (CCDC78)
ENST00000466708.5:n.1371A>T (CCDC78)
ENST00000478979.5:n.1505A>T (CCDC78)
ENST00000481804.5:n.2005A>T (CCDC78)
ENST00000482152.1:n.388A>T (CCDC78)
ENST00000482878.5:n.1908A>T (CCDC78)
ENST00000485091.5:n.1180A>T (CCDC78)
ENST00000620831.4:c.-49-38500T>A (MSLN)	ENSP00000482893.1:n.-49-38500T>A
NM_001031737.2:c.1027A>T (CCDC78)	NP_001026907.2:p.Thr343Ser
XM_006720838.1:c.1249A>T (CCDC78)	XP_006720901.1:p.Thr417Ser
XM_006720843.2:c.1027A>T (CCDC78)	XP_006720906.1:p.Thr343Ser
XM_011522356.1:c.1474A>T (CCDC78)	XP_011520658.1:p.Thr492Ser
XM_011522357.1:c.1462A>T (CCDC78)	XP_011520659.1:p.Thr488Ser
XM_011522358.1:c.1474A>T (CCDC78)	XP_011520660.1:p.Thr492Ser
XM_011522359.1:c.1441A>T (CCDC78)	XP_011520661.1:p.Thr481Ser
XM_011522360.1:c.1429A>T (CCDC78)	XP_011520662.1:p.Thr477Ser
XM_011522361.1:c.1474A>T (CCDC78)	XP_011520663.1:p.Thr492Ser
XM_011522362.1:c.1474A>T (CCDC78)	XP_011520664.1:p.Thr492Ser
XM_011522363.1:c.1474A>T (CCDC78)	XP_011520665.1:p.Thr492Ser
XM_011522364.1:c.1474A>T (CCDC78)	XP_011520666.1:p.Thr492Ser
XM_011522365.1:c.1261A>T (CCDC78)	XP_011520667.1:p.Thr421Ser
XM_011522366.1:c.1252A>T (CCDC78)	XP_011520668.1:p.Thr418Ser
XM_011522367.1:c.1093A>T (CCDC78)	XP_011520669.1:p.Thr365Ser
XM_011522368.1:c.1081A>T (CCDC78)	XP_011520670.1:p.Thr361Ser
XM_011522369.1:c.1039A>T (CCDC78)	XP_011520671.1:p.Thr347Ser
XM_011522370.1:c.871A>T (CCDC78)	XP_011520672.1:p.Thr291Ser
XM_011522371.1:c.586A>T (CCDC78)	XP_011520673.1:p.Thr196Ser
XM_006720843.4:c.1027A>T (CCDC78)	XP_006720906.1:p.Thr343Ser
XM_011522358.2:c.1474A>T (CCDC78)	XP_011520660.1:p.Thr492Ser
XM_011522371.2:c.586A>T (CCDC78)	XP_011520673.1:p.Thr196Ser
XM_017022929.1:c.1474A>T (CCDC78)	XP_016878418.1:p.Thr492Ser
XM_017022930.1:c.574A>T (CCDC78)	XP_016878419.1:p.Thr192Ser
XM_024450150.1:c.304A>T (CCDC78)	XP_024305918.1:p.Thr102Ser
XR_001751835.1:n.1813A>T (CCDC78)
XR_001751836.1:n.1792A>T (CCDC78)
XR_001751837.1:n.1570A>T (CCDC78)
XR_001751838.1:n.1916A>T (CCDC78)
XR_001751839.1:n.1378A>T (CCDC78)
NM_001031737.3:c.1027A>T (CCDC78)	NP_001026907.2:p.Thr343Ser
NM_001378030.1:c.1027A>T (CCDC78) MANE Select	NP_001364959.1:p.Thr343Ser
NM_001378031.1:c.953+190A>T (CCDC78)	NP_001364960.1:n.953+190A>T
NM_001378033.1:c.460A>T (CCDC78)	NP_001364962.1:p.Thr154Ser
NR_165382.1:n.1584A>T (CCDC78)
NR_165383.1:n.1230A>T (CCDC78)
NR_165384.1:n.1195A>T (CCDC78)
NR_165385.1:n.1295A>T (CCDC78)
NR_165386.1:n.1362A>T (CCDC78)