Canonical Allele Identifier: CA492830066

Linked Data

MyVariant Identifiers: chr16:g.773910T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.723910T>G , CM000678.2:g.723910T>G GRCh38
NC_000016.9:g.773910T>G , CM000678.1:g.773910T>G GRCh37
NC_000016.8:g.713911T>G NCBI36
NG_032932.1:g.7564A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682391.1:n.1623A>C (CCDC78)
ENST00000345165.10:c.1080A>C (CCDC78) MANE Select ENSP00000316851.5:p.Ser360=
ENST00000293889.10:c.1080A>C (CCDC78) ENSP00000293889.6:p.Ser360=
ENST00000345165.8:c.626A>C (CCDC78)
ENST00000463539.5:n.1402A>C (CCDC78)
ENST00000466708.5:n.1424A>C (CCDC78)
ENST00000478979.5:n.1727A>C (CCDC78)
ENST00000481804.5:n.2058A>C (CCDC78)
ENST00000482152.1:n.441A>C (CCDC78)
ENST00000482878.5:n.2130A>C (CCDC78)
ENST00000485091.5:n.1233A>C (CCDC78)
ENST00000620831.4:c.-49-38722T>G (MSLN) ENSP00000482893.1:n.-49-38722T>G
NM_001031737.2:c.1080A>C (CCDC78) NP_001026907.2:p.Ser360=
XM_006720838.1:c.1302A>C (CCDC78) XP_006720901.1:p.Ser434=
XM_006720843.2:c.1080A>C (CCDC78) XP_006720906.1:p.Ser360=
XM_011522356.1:c.1527A>C (CCDC78) XP_011520658.1:p.Ser509=
XM_011522357.1:c.1515A>C (CCDC78) XP_011520659.1:p.Ser505=
XM_011522358.1:c.1527A>C (CCDC78) XP_011520660.1:p.Ser509=
XM_011522359.1:c.1494A>C (CCDC78) XP_011520661.1:p.Ser498=
XM_011522360.1:c.1482A>C (CCDC78) XP_011520662.1:p.Ser494=
XM_011522361.1:c.1527A>C (CCDC78) XP_011520663.1:p.Ser509=
XM_011522362.1:c.1527A>C (CCDC78) XP_011520664.1:p.Ser509=
XM_011522363.1:c.1527A>C (CCDC78) XP_011520665.1:p.Ser509=
XM_011522364.1:c.1527A>C (CCDC78) XP_011520666.1:p.Ser509=
XM_011522365.1:c.1314A>C (CCDC78) XP_011520667.1:p.Ser438=
XM_011522366.1:c.1305A>C (CCDC78) XP_011520668.1:p.Ser435=
XM_011522367.1:c.1146A>C (CCDC78) XP_011520669.1:p.Ser382=
XM_011522368.1:c.1134A>C (CCDC78) XP_011520670.1:p.Ser378=
XM_011522369.1:c.1092A>C (CCDC78) XP_011520671.1:p.Ser364=
XM_011522370.1:c.924A>C (CCDC78) XP_011520672.1:p.Ser308=
XM_011522371.1:c.639A>C (CCDC78) XP_011520673.1:p.Ser213=
XM_006720843.4:c.1080A>C (CCDC78) XP_006720906.1:p.Ser360=
XM_011522358.2:c.1527A>C (CCDC78) XP_011520660.1:p.Ser509=
XM_011522371.2:c.639A>C (CCDC78) XP_011520673.1:p.Ser213=
XM_017022929.1:c.1527A>C (CCDC78) XP_016878418.1:p.Ser509=
XM_017022930.1:c.627A>C (CCDC78) XP_016878419.1:p.Ser209=
XM_017022931.1:c.-174A>C (CCDC78) XP_016878420.1:n.-174A>C
XM_024450150.1:c.357A>C (CCDC78) XP_024305918.1:p.Ser119=
XR_001751835.1:n.1866A>C (CCDC78)
XR_001751836.1:n.1845A>C (CCDC78)
XR_001751837.1:n.1623A>C (CCDC78)
XR_001751838.1:n.1969A>C (CCDC78)
XR_001751839.1:n.1431A>C (CCDC78)
NM_001031737.3:c.1080A>C (CCDC78) NP_001026907.2:p.Ser360=
NM_001378030.1:c.1080A>C (CCDC78) MANE Select NP_001364959.1:p.Ser360=
NM_001378031.1:c.953+412A>C (CCDC78) NP_001364960.1:n.953+412A>C
NM_001378033.1:c.513A>C (CCDC78) NP_001364962.1:p.Ser171=
NR_165382.1:n.1637A>C (CCDC78)
NR_165383.1:n.1283A>C (CCDC78)
NR_165384.1:n.1248A>C (CCDC78)
NR_165385.1:n.1348A>C (CCDC78)
NR_165386.1:n.1415A>C (CCDC78)