Canonical Allele Identifier: CA492830036

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.773868T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723868T>G , CM000678.2:g.723868T>G	GRCh38
NC_000016.9:g.773868T>G , CM000678.1:g.773868T>G	GRCh37
NC_000016.8:g.713869T>G	NCBI36
NG_032932.1:g.7606A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1665A>C (CCDC78)
ENST00000345165.10:c.1122A>C (CCDC78) MANE Select	ENSP00000316851.5:p.Thr374=
ENST00000293889.10:c.1122A>C (CCDC78)	ENSP00000293889.6:p.Thr374=
ENST00000345165.8:c.668A>C (CCDC78)
ENST00000463539.5:n.1444A>C (CCDC78)
ENST00000466708.5:n.1466A>C (CCDC78)
ENST00000478979.5:n.1769A>C (CCDC78)
ENST00000481804.5:n.2100A>C (CCDC78)
ENST00000482152.1:n.483A>C (CCDC78)
ENST00000482878.5:n.2172A>C (CCDC78)
ENST00000485091.5:n.1275A>C (CCDC78)
ENST00000620831.4:c.-49-38764T>G (MSLN)	ENSP00000482893.1:n.-49-38764T>G
NM_001031737.2:c.1122A>C (CCDC78)	NP_001026907.2:p.Thr374=
XM_006720838.1:c.1344A>C (CCDC78)	XP_006720901.1:p.Thr448=
XM_006720843.2:c.1122A>C (CCDC78)	XP_006720906.1:p.Thr374=
XM_011522356.1:c.1569A>C (CCDC78)	XP_011520658.1:p.Thr523=
XM_011522357.1:c.1557A>C (CCDC78)	XP_011520659.1:p.Thr519=
XM_011522358.1:c.1569A>C (CCDC78)	XP_011520660.1:p.Thr523=
XM_011522359.1:c.1536A>C (CCDC78)	XP_011520661.1:p.Thr512=
XM_011522360.1:c.1524A>C (CCDC78)	XP_011520662.1:p.Thr508=
XM_011522361.1:c.1569A>C (CCDC78)	XP_011520663.1:p.Thr523=
XM_011522362.1:c.1569A>C (CCDC78)	XP_011520664.1:p.Thr523=
XM_011522363.1:c.1569A>C (CCDC78)	XP_011520665.1:p.Thr523=
XM_011522364.1:c.1569A>C (CCDC78)	XP_011520666.1:p.Thr523=
XM_011522365.1:c.1356A>C (CCDC78)	XP_011520667.1:p.Thr452=
XM_011522366.1:c.1347A>C (CCDC78)	XP_011520668.1:p.Thr449=
XM_011522367.1:c.1188A>C (CCDC78)	XP_011520669.1:p.Thr396=
XM_011522368.1:c.1176A>C (CCDC78)	XP_011520670.1:p.Thr392=
XM_011522369.1:c.1134A>C (CCDC78)	XP_011520671.1:p.Thr378=
XM_011522370.1:c.966A>C (CCDC78)	XP_011520672.1:p.Thr322=
XM_011522371.1:c.681A>C (CCDC78)	XP_011520673.1:p.Thr227=
XM_006720843.4:c.1122A>C (CCDC78)	XP_006720906.1:p.Thr374=
XM_011522358.2:c.1569A>C (CCDC78)	XP_011520660.1:p.Thr523=
XM_011522371.2:c.681A>C (CCDC78)	XP_011520673.1:p.Thr227=
XM_017022929.1:c.1569A>C (CCDC78)	XP_016878418.1:p.Thr523=
XM_017022930.1:c.669A>C (CCDC78)	XP_016878419.1:p.Thr223=
XM_017022931.1:c.-132A>C (CCDC78)	XP_016878420.1:n.-132A>C
XM_024450150.1:c.399A>C (CCDC78)	XP_024305918.1:p.Thr133=
XR_001751835.1:n.1908A>C (CCDC78)
XR_001751836.1:n.1887A>C (CCDC78)
XR_001751837.1:n.1665A>C (CCDC78)
XR_001751838.1:n.2011A>C (CCDC78)
XR_001751839.1:n.1473A>C (CCDC78)
NM_001031737.3:c.1122A>C (CCDC78)	NP_001026907.2:p.Thr374=
NM_001378030.1:c.1122A>C (CCDC78) MANE Select	NP_001364959.1:p.Thr374=
NM_001378031.1:c.953+454A>C (CCDC78)	NP_001364960.1:n.953+454A>C
NM_001378033.1:c.555A>C (CCDC78)	NP_001364962.1:p.Thr185=
NR_165382.1:n.1679A>C (CCDC78)
NR_165383.1:n.1325A>C (CCDC78)
NR_165384.1:n.1290A>C (CCDC78)
NR_165385.1:n.1390A>C (CCDC78)
NR_165386.1:n.1457A>C (CCDC78)