Canonical Allele Identifier: CA2201211335

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.723884G= , CM000678.2:g.723884G= GRCh38
NC_000016.9:g.773884G= , CM000678.1:g.773884G= GRCh37
NC_000016.8:g.713885G= NCBI36
NG_032932.1:g.7590C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682391.1:n.1649C= (CCDC78)
ENST00000345165.10:c.1106C= (CCDC78) MANE Select ENSP00000316851.5:p.Ala369=
ENST00000293889.10:c.1106C= (CCDC78) ENSP00000293889.6:p.Ala369=
ENST00000345165.8:c.652C= (CCDC78)
ENST00000463539.5:n.1428C= (CCDC78)
ENST00000466708.5:n.1450C= (CCDC78)
ENST00000478979.5:n.1753C= (CCDC78)
ENST00000481804.5:n.2084C= (CCDC78)
ENST00000482152.1:n.467C= (CCDC78)
ENST00000482878.5:n.2156C= (CCDC78)
ENST00000485091.5:n.1259C= (CCDC78)
ENST00000620831.4:c.-49-38748G= (MSLN) ENSP00000482893.1:n.-49-38748G=
NM_001031737.2:c.1106C= (CCDC78) NP_001026907.2:p.Ala369=
XM_006720838.1:c.1328C= (CCDC78) XP_006720901.1:p.Ala443=
XM_006720843.2:c.1106C= (CCDC78) XP_006720906.1:p.Ala369=
XM_011522356.1:c.1553C= (CCDC78) XP_011520658.1:p.Ala518=
XM_011522357.1:c.1541C= (CCDC78) XP_011520659.1:p.Ala514=
XM_011522358.1:c.1553C= (CCDC78) XP_011520660.1:p.Ala518=
XM_011522359.1:c.1520C= (CCDC78) XP_011520661.1:p.Ala507=
XM_011522360.1:c.1508C= (CCDC78) XP_011520662.1:p.Ala503=
XM_011522361.1:c.1553C= (CCDC78) XP_011520663.1:p.Ala518=
XM_011522362.1:c.1553C= (CCDC78) XP_011520664.1:p.Ala518=
XM_011522363.1:c.1553C= (CCDC78) XP_011520665.1:p.Ala518=
XM_011522364.1:c.1553C= (CCDC78) XP_011520666.1:p.Ala518=
XM_011522365.1:c.1340C= (CCDC78) XP_011520667.1:p.Ala447=
XM_011522366.1:c.1331C= (CCDC78) XP_011520668.1:p.Ala444=
XM_011522367.1:c.1172C= (CCDC78) XP_011520669.1:p.Ala391=
XM_011522368.1:c.1160C= (CCDC78) XP_011520670.1:p.Ala387=
XM_011522369.1:c.1118C= (CCDC78) XP_011520671.1:p.Ala373=
XM_011522370.1:c.950C= (CCDC78) XP_011520672.1:p.Ala317=
XM_011522371.1:c.665C= (CCDC78) XP_011520673.1:p.Ala222=
XM_006720843.4:c.1106C= (CCDC78) XP_006720906.1:p.Ala369=
XM_011522358.2:c.1553C= (CCDC78) XP_011520660.1:p.Ala518=
XM_011522371.2:c.665C= (CCDC78) XP_011520673.1:p.Ala222=
XM_017022929.1:c.1553C= (CCDC78) XP_016878418.1:p.Ala518=
XM_017022930.1:c.653C= (CCDC78) XP_016878419.1:p.Ala218=
XM_017022931.1:c.-148C= (CCDC78) XP_016878420.1:n.-148C=
XM_024450150.1:c.383C= (CCDC78) XP_024305918.1:p.Ala128=
XR_001751835.1:n.1892C= (CCDC78)
XR_001751836.1:n.1871C= (CCDC78)
XR_001751837.1:n.1649C= (CCDC78)
XR_001751838.1:n.1995C= (CCDC78)
XR_001751839.1:n.1457C= (CCDC78)
NM_001031737.3:c.1106C= (CCDC78) NP_001026907.2:p.Ala369=
NM_001378030.1:c.1106C= (CCDC78) MANE Select NP_001364959.1:p.Ala369=
NM_001378031.1:c.953+438C= (CCDC78) NP_001364960.1:n.953+438C=
NM_001378033.1:c.539C= (CCDC78) NP_001364962.1:p.Ala180=
NR_165382.1:n.1663C= (CCDC78)
NR_165383.1:n.1309C= (CCDC78)
NR_165384.1:n.1274C= (CCDC78)
NR_165385.1:n.1374C= (CCDC78)
NR_165386.1:n.1441C= (CCDC78)