Canonical Allele Identifier: CA2201211326

Gene: CCDC78 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723867A= , CM000678.2:g.723867A=	GRCh38
NC_000016.9:g.773867A= , CM000678.1:g.773867A=	GRCh37
NC_000016.8:g.713868A=	NCBI36
NG_032932.1:g.7607T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1666T= (CCDC78)
ENST00000345165.10:c.1123T= (CCDC78) MANE Select	ENSP00000316851.5:p.Ser375=
ENST00000293889.10:c.1123T= (CCDC78)	ENSP00000293889.6:p.Ser375=
ENST00000345165.8:c.669T= (CCDC78)
ENST00000463539.5:n.1445T= (CCDC78)
ENST00000466708.5:n.1467T= (CCDC78)
ENST00000478979.5:n.1770T= (CCDC78)
ENST00000481804.5:n.2101T= (CCDC78)
ENST00000482152.1:n.484T= (CCDC78)
ENST00000482878.5:n.2173T= (CCDC78)
ENST00000485091.5:n.1276T= (CCDC78)
ENST00000620831.4:c.-49-38765A= (MSLN)	ENSP00000482893.1:n.-49-38765A=
NM_001031737.2:c.1123T= (CCDC78)	NP_001026907.2:p.Ser375=
XM_006720838.1:c.1345T= (CCDC78)	XP_006720901.1:p.Ser449=
XM_006720843.2:c.1123T= (CCDC78)	XP_006720906.1:p.Ser375=
XM_011522356.1:c.1570T= (CCDC78)	XP_011520658.1:p.Ser524=
XM_011522357.1:c.1558T= (CCDC78)	XP_011520659.1:p.Ser520=
XM_011522358.1:c.1570T= (CCDC78)	XP_011520660.1:p.Ser524=
XM_011522359.1:c.1537T= (CCDC78)	XP_011520661.1:p.Ser513=
XM_011522360.1:c.1525T= (CCDC78)	XP_011520662.1:p.Ser509=
XM_011522361.1:c.1570T= (CCDC78)	XP_011520663.1:p.Ser524=
XM_011522362.1:c.1570T= (CCDC78)	XP_011520664.1:p.Ser524=
XM_011522363.1:c.1570T= (CCDC78)	XP_011520665.1:p.Ser524=
XM_011522364.1:c.1570T= (CCDC78)	XP_011520666.1:p.Ser524=
XM_011522365.1:c.1357T= (CCDC78)	XP_011520667.1:p.Ser453=
XM_011522366.1:c.1348T= (CCDC78)	XP_011520668.1:p.Ser450=
XM_011522367.1:c.1189T= (CCDC78)	XP_011520669.1:p.Ser397=
XM_011522368.1:c.1177T= (CCDC78)	XP_011520670.1:p.Ser393=
XM_011522369.1:c.1135T= (CCDC78)	XP_011520671.1:p.Ser379=
XM_011522370.1:c.967T= (CCDC78)	XP_011520672.1:p.Ser323=
XM_011522371.1:c.682T= (CCDC78)	XP_011520673.1:p.Ser228=
XM_006720843.4:c.1123T= (CCDC78)	XP_006720906.1:p.Ser375=
XM_011522358.2:c.1570T= (CCDC78)	XP_011520660.1:p.Ser524=
XM_011522371.2:c.682T= (CCDC78)	XP_011520673.1:p.Ser228=
XM_017022929.1:c.1570T= (CCDC78)	XP_016878418.1:p.Ser524=
XM_017022930.1:c.670T= (CCDC78)	XP_016878419.1:p.Ser224=
XM_017022931.1:c.-131T= (CCDC78)	XP_016878420.1:n.-131T=
XM_024450150.1:c.400T= (CCDC78)	XP_024305918.1:p.Ser134=
XR_001751835.1:n.1909T= (CCDC78)
XR_001751836.1:n.1888T= (CCDC78)
XR_001751837.1:n.1666T= (CCDC78)
XR_001751838.1:n.2012T= (CCDC78)
XR_001751839.1:n.1474T= (CCDC78)
NM_001031737.3:c.1123T= (CCDC78)	NP_001026907.2:p.Ser375=
NM_001378030.1:c.1123T= (CCDC78) MANE Select	NP_001364959.1:p.Ser375=
NM_001378031.1:c.953+455T= (CCDC78)	NP_001364960.1:n.953+455T=
NM_001378033.1:c.556T= (CCDC78)	NP_001364962.1:p.Ser186=
NR_165382.1:n.1680T= (CCDC78)
NR_165383.1:n.1326T= (CCDC78)
NR_165384.1:n.1291T= (CCDC78)
NR_165385.1:n.1391T= (CCDC78)
NR_165386.1:n.1458T= (CCDC78)