Canonical Allele Identifier: CA394098412

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.723901T>A , CM000678.2:g.723901T>A GRCh38
NC_000016.9:g.773901T>A , CM000678.1:g.773901T>A GRCh37
NC_000016.8:g.713902T>A NCBI36
NG_032932.1:g.7573A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682391.1:n.1632A>T (CCDC78)
ENST00000345165.10:c.1089A>T (CCDC78) MANE Select ENSP00000316851.5:p.Lys363Asn
ENST00000293889.10:c.1089A>T (CCDC78) ENSP00000293889.6:p.Lys363Asn
ENST00000345165.8:c.635A>T (CCDC78)
ENST00000463539.5:n.1411A>T (CCDC78)
ENST00000466708.5:n.1433A>T (CCDC78)
ENST00000478979.5:n.1736A>T (CCDC78)
ENST00000481804.5:n.2067A>T (CCDC78)
ENST00000482152.1:n.450A>T (CCDC78)
ENST00000482878.5:n.2139A>T (CCDC78)
ENST00000485091.5:n.1242A>T (CCDC78)
ENST00000620831.4:c.-49-38731T>A (MSLN) ENSP00000482893.1:n.-49-38731T>A
NM_001031737.2:c.1089A>T (CCDC78) NP_001026907.2:p.Lys363Asn
XM_006720838.1:c.1311A>T (CCDC78) XP_006720901.1:p.Lys437Asn
XM_006720843.2:c.1089A>T (CCDC78) XP_006720906.1:p.Lys363Asn
XM_011522356.1:c.1536A>T (CCDC78) XP_011520658.1:p.Lys512Asn
XM_011522357.1:c.1524A>T (CCDC78) XP_011520659.1:p.Lys508Asn
XM_011522358.1:c.1536A>T (CCDC78) XP_011520660.1:p.Lys512Asn
XM_011522359.1:c.1503A>T (CCDC78) XP_011520661.1:p.Lys501Asn
XM_011522360.1:c.1491A>T (CCDC78) XP_011520662.1:p.Lys497Asn
XM_011522361.1:c.1536A>T (CCDC78) XP_011520663.1:p.Lys512Asn
XM_011522362.1:c.1536A>T (CCDC78) XP_011520664.1:p.Lys512Asn
XM_011522363.1:c.1536A>T (CCDC78) XP_011520665.1:p.Lys512Asn
XM_011522364.1:c.1536A>T (CCDC78) XP_011520666.1:p.Lys512Asn
XM_011522365.1:c.1323A>T (CCDC78) XP_011520667.1:p.Lys441Asn
XM_011522366.1:c.1314A>T (CCDC78) XP_011520668.1:p.Lys438Asn
XM_011522367.1:c.1155A>T (CCDC78) XP_011520669.1:p.Lys385Asn
XM_011522368.1:c.1143A>T (CCDC78) XP_011520670.1:p.Lys381Asn
XM_011522369.1:c.1101A>T (CCDC78) XP_011520671.1:p.Lys367Asn
XM_011522370.1:c.933A>T (CCDC78) XP_011520672.1:p.Lys311Asn
XM_011522371.1:c.648A>T (CCDC78) XP_011520673.1:p.Lys216Asn
XM_006720843.4:c.1089A>T (CCDC78) XP_006720906.1:p.Lys363Asn
XM_011522358.2:c.1536A>T (CCDC78) XP_011520660.1:p.Lys512Asn
XM_011522371.2:c.648A>T (CCDC78) XP_011520673.1:p.Lys216Asn
XM_017022929.1:c.1536A>T (CCDC78) XP_016878418.1:p.Lys512Asn
XM_017022930.1:c.636A>T (CCDC78) XP_016878419.1:p.Lys212Asn
XM_017022931.1:c.-165A>T (CCDC78) XP_016878420.1:n.-165A>T
XM_024450150.1:c.366A>T (CCDC78) XP_024305918.1:p.Lys122Asn
XR_001751835.1:n.1875A>T (CCDC78)
XR_001751836.1:n.1854A>T (CCDC78)
XR_001751837.1:n.1632A>T (CCDC78)
XR_001751838.1:n.1978A>T (CCDC78)
XR_001751839.1:n.1440A>T (CCDC78)
NM_001031737.3:c.1089A>T (CCDC78) NP_001026907.2:p.Lys363Asn
NM_001378030.1:c.1089A>T (CCDC78) MANE Select NP_001364959.1:p.Lys363Asn
NM_001378031.1:c.953+421A>T (CCDC78) NP_001364960.1:n.953+421A>T
NM_001378033.1:c.522A>T (CCDC78) NP_001364962.1:p.Lys174Asn
NR_165382.1:n.1646A>T (CCDC78)
NR_165383.1:n.1292A>T (CCDC78)
NR_165384.1:n.1257A>T (CCDC78)
NR_165385.1:n.1357A>T (CCDC78)
NR_165386.1:n.1424A>T (CCDC78)