Canonical Allele Identifier: CA394098892

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.774143A>T (hg19) ; chr16:g.724143A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724143A>T , CM000678.2:g.724143A>T	GRCh38
NC_000016.9:g.774143A>T , CM000678.1:g.774143A>T	GRCh37
NC_000016.8:g.714144A>T	NCBI36
NG_032932.1:g.7331T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1559T>A (CCDC78)
ENST00000345165.10:c.1016T>A (CCDC78) MANE Select	ENSP00000316851.5:p.Val339Glu
ENST00000293889.10:c.1016T>A (CCDC78)	ENSP00000293889.6:p.Val339Glu
ENST00000345165.8:c.562T>A (CCDC78)
ENST00000463539.5:n.1338T>A (CCDC78)
ENST00000466708.5:n.1360T>A (CCDC78)
ENST00000478979.5:n.1494T>A (CCDC78)
ENST00000481804.5:n.1994T>A (CCDC78)
ENST00000482152.1:n.377T>A (CCDC78)
ENST00000482878.5:n.1897T>A (CCDC78)
ENST00000485091.5:n.1169T>A (CCDC78)
ENST00000620831.4:c.-49-38489A>T (MSLN)	ENSP00000482893.1:n.-49-38489A>T
NM_001031737.2:c.1016T>A (CCDC78)	NP_001026907.2:p.Val339Glu
XM_006720838.1:c.1238T>A (CCDC78)	XP_006720901.1:p.Val413Glu
XM_006720843.2:c.1016T>A (CCDC78)	XP_006720906.1:p.Val339Glu
XM_011522356.1:c.1463T>A (CCDC78)	XP_011520658.1:p.Val488Glu
XM_011522357.1:c.1451T>A (CCDC78)	XP_011520659.1:p.Val484Glu
XM_011522358.1:c.1463T>A (CCDC78)	XP_011520660.1:p.Val488Glu
XM_011522359.1:c.1430T>A (CCDC78)	XP_011520661.1:p.Val477Glu
XM_011522360.1:c.1418T>A (CCDC78)	XP_011520662.1:p.Val473Glu
XM_011522361.1:c.1463T>A (CCDC78)	XP_011520663.1:p.Val488Glu
XM_011522362.1:c.1463T>A (CCDC78)	XP_011520664.1:p.Val488Glu
XM_011522363.1:c.1463T>A (CCDC78)	XP_011520665.1:p.Val488Glu
XM_011522364.1:c.1463T>A (CCDC78)	XP_011520666.1:p.Val488Glu
XM_011522365.1:c.1250T>A (CCDC78)	XP_011520667.1:p.Val417Glu
XM_011522366.1:c.1241T>A (CCDC78)	XP_011520668.1:p.Val414Glu
XM_011522367.1:c.1082T>A (CCDC78)	XP_011520669.1:p.Val361Glu
XM_011522368.1:c.1070T>A (CCDC78)	XP_011520670.1:p.Val357Glu
XM_011522369.1:c.1028T>A (CCDC78)	XP_011520671.1:p.Val343Glu
XM_011522370.1:c.860T>A (CCDC78)	XP_011520672.1:p.Val287Glu
XM_011522371.1:c.575T>A (CCDC78)	XP_011520673.1:p.Val192Glu
XM_006720843.4:c.1016T>A (CCDC78)	XP_006720906.1:p.Val339Glu
XM_011522358.2:c.1463T>A (CCDC78)	XP_011520660.1:p.Val488Glu
XM_011522371.2:c.575T>A (CCDC78)	XP_011520673.1:p.Val192Glu
XM_017022929.1:c.1463T>A (CCDC78)	XP_016878418.1:p.Val488Glu
XM_017022930.1:c.563T>A (CCDC78)	XP_016878419.1:p.Val188Glu
XM_024450150.1:c.293T>A (CCDC78)	XP_024305918.1:p.Val98Glu
XR_001751835.1:n.1802T>A (CCDC78)
XR_001751836.1:n.1781T>A (CCDC78)
XR_001751837.1:n.1559T>A (CCDC78)
XR_001751838.1:n.1905T>A (CCDC78)
XR_001751839.1:n.1367T>A (CCDC78)
NM_001031737.3:c.1016T>A (CCDC78)	NP_001026907.2:p.Val339Glu
NM_001378030.1:c.1016T>A (CCDC78) MANE Select	NP_001364959.1:p.Val339Glu
NM_001378031.1:c.953+179T>A (CCDC78)	NP_001364960.1:n.953+179T>A
NM_001378033.1:c.449T>A (CCDC78)	NP_001364962.1:p.Val150Glu
NR_165382.1:n.1573T>A (CCDC78)
NR_165383.1:n.1219T>A (CCDC78)
NR_165384.1:n.1184T>A (CCDC78)
NR_165385.1:n.1284T>A (CCDC78)
NR_165386.1:n.1351T>A (CCDC78)