Canonical Allele Identifier: CA394098799

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.774126A>T (hg19) ; chr16:g.724126A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724126A>T , CM000678.2:g.724126A>T	GRCh38
NC_000016.9:g.774126A>T , CM000678.1:g.774126A>T	GRCh37
NC_000016.8:g.714127A>T	NCBI36
NG_032932.1:g.7348T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1576T>A (CCDC78)
ENST00000345165.10:c.1033T>A (CCDC78) MANE Select	ENSP00000316851.5:p.Phe345Ile
ENST00000293889.10:c.1033T>A (CCDC78)	ENSP00000293889.6:p.Phe345Ile
ENST00000345165.8:c.579T>A (CCDC78)
ENST00000463539.5:n.1355T>A (CCDC78)
ENST00000466708.5:n.1377T>A (CCDC78)
ENST00000478979.5:n.1511T>A (CCDC78)
ENST00000481804.5:n.2011T>A (CCDC78)
ENST00000482152.1:n.394T>A (CCDC78)
ENST00000482878.5:n.1914T>A (CCDC78)
ENST00000485091.5:n.1186T>A (CCDC78)
ENST00000620831.4:c.-49-38506A>T (MSLN)	ENSP00000482893.1:n.-49-38506A>T
NM_001031737.2:c.1033T>A (CCDC78)	NP_001026907.2:p.Phe345Ile
XM_006720838.1:c.1255T>A (CCDC78)	XP_006720901.1:p.Phe419Ile
XM_006720843.2:c.1033T>A (CCDC78)	XP_006720906.1:p.Phe345Ile
XM_011522356.1:c.1480T>A (CCDC78)	XP_011520658.1:p.Phe494Ile
XM_011522357.1:c.1468T>A (CCDC78)	XP_011520659.1:p.Phe490Ile
XM_011522358.1:c.1480T>A (CCDC78)	XP_011520660.1:p.Phe494Ile
XM_011522359.1:c.1447T>A (CCDC78)	XP_011520661.1:p.Phe483Ile
XM_011522360.1:c.1435T>A (CCDC78)	XP_011520662.1:p.Phe479Ile
XM_011522361.1:c.1480T>A (CCDC78)	XP_011520663.1:p.Phe494Ile
XM_011522362.1:c.1480T>A (CCDC78)	XP_011520664.1:p.Phe494Ile
XM_011522363.1:c.1480T>A (CCDC78)	XP_011520665.1:p.Phe494Ile
XM_011522364.1:c.1480T>A (CCDC78)	XP_011520666.1:p.Phe494Ile
XM_011522365.1:c.1267T>A (CCDC78)	XP_011520667.1:p.Phe423Ile
XM_011522366.1:c.1258T>A (CCDC78)	XP_011520668.1:p.Phe420Ile
XM_011522367.1:c.1099T>A (CCDC78)	XP_011520669.1:p.Phe367Ile
XM_011522368.1:c.1087T>A (CCDC78)	XP_011520670.1:p.Phe363Ile
XM_011522369.1:c.1045T>A (CCDC78)	XP_011520671.1:p.Phe349Ile
XM_011522370.1:c.877T>A (CCDC78)	XP_011520672.1:p.Phe293Ile
XM_011522371.1:c.592T>A (CCDC78)	XP_011520673.1:p.Phe198Ile
XM_006720843.4:c.1033T>A (CCDC78)	XP_006720906.1:p.Phe345Ile
XM_011522358.2:c.1480T>A (CCDC78)	XP_011520660.1:p.Phe494Ile
XM_011522371.2:c.592T>A (CCDC78)	XP_011520673.1:p.Phe198Ile
XM_017022929.1:c.1480T>A (CCDC78)	XP_016878418.1:p.Phe494Ile
XM_017022930.1:c.580T>A (CCDC78)	XP_016878419.1:p.Phe194Ile
XM_024450150.1:c.310T>A (CCDC78)	XP_024305918.1:p.Phe104Ile
XR_001751835.1:n.1819T>A (CCDC78)
XR_001751836.1:n.1798T>A (CCDC78)
XR_001751837.1:n.1576T>A (CCDC78)
XR_001751838.1:n.1922T>A (CCDC78)
XR_001751839.1:n.1384T>A (CCDC78)
NM_001031737.3:c.1033T>A (CCDC78)	NP_001026907.2:p.Phe345Ile
NM_001378030.1:c.1033T>A (CCDC78) MANE Select	NP_001364959.1:p.Phe345Ile
NM_001378031.1:c.953+196T>A (CCDC78)	NP_001364960.1:n.953+196T>A
NM_001378033.1:c.466T>A (CCDC78)	NP_001364962.1:p.Phe156Ile
NR_165382.1:n.1590T>A (CCDC78)
NR_165383.1:n.1236T>A (CCDC78)
NR_165384.1:n.1201T>A (CCDC78)
NR_165385.1:n.1301T>A (CCDC78)
NR_165386.1:n.1368T>A (CCDC78)