Canonical Allele Identifier: CA394098841

Gene: CCDC78 MSLN

Linked Data

• COSMIC: COSM342852
• MyVariant Identifiers: chr16:g.774131G>T (hg19) ; chr16:g.724131G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724131G>T , CM000678.2:g.724131G>T	GRCh38
NC_000016.9:g.774131G>T , CM000678.1:g.774131G>T	GRCh37
NC_000016.8:g.714132G>T	NCBI36
NG_032932.1:g.7343C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1571C>A (CCDC78)
ENST00000345165.10:c.1028C>A (CCDC78) MANE Select	ENSP00000316851.5:p.Thr343Asn
ENST00000293889.10:c.1028C>A (CCDC78)	ENSP00000293889.6:p.Thr343Asn
ENST00000345165.8:c.574C>A (CCDC78)
ENST00000463539.5:n.1350C>A (CCDC78)
ENST00000466708.5:n.1372C>A (CCDC78)
ENST00000478979.5:n.1506C>A (CCDC78)
ENST00000481804.5:n.2006C>A (CCDC78)
ENST00000482152.1:n.389C>A (CCDC78)
ENST00000482878.5:n.1909C>A (CCDC78)
ENST00000485091.5:n.1181C>A (CCDC78)
ENST00000620831.4:c.-49-38501G>T (MSLN)	ENSP00000482893.1:n.-49-38501G>T
NM_001031737.2:c.1028C>A (CCDC78)	NP_001026907.2:p.Thr343Asn
XM_006720838.1:c.1250C>A (CCDC78)	XP_006720901.1:p.Thr417Asn
XM_006720843.2:c.1028C>A (CCDC78)	XP_006720906.1:p.Thr343Asn
XM_011522356.1:c.1475C>A (CCDC78)	XP_011520658.1:p.Thr492Asn
XM_011522357.1:c.1463C>A (CCDC78)	XP_011520659.1:p.Thr488Asn
XM_011522358.1:c.1475C>A (CCDC78)	XP_011520660.1:p.Thr492Asn
XM_011522359.1:c.1442C>A (CCDC78)	XP_011520661.1:p.Thr481Asn
XM_011522360.1:c.1430C>A (CCDC78)	XP_011520662.1:p.Thr477Asn
XM_011522361.1:c.1475C>A (CCDC78)	XP_011520663.1:p.Thr492Asn
XM_011522362.1:c.1475C>A (CCDC78)	XP_011520664.1:p.Thr492Asn
XM_011522363.1:c.1475C>A (CCDC78)	XP_011520665.1:p.Thr492Asn
XM_011522364.1:c.1475C>A (CCDC78)	XP_011520666.1:p.Thr492Asn
XM_011522365.1:c.1262C>A (CCDC78)	XP_011520667.1:p.Thr421Asn
XM_011522366.1:c.1253C>A (CCDC78)	XP_011520668.1:p.Thr418Asn
XM_011522367.1:c.1094C>A (CCDC78)	XP_011520669.1:p.Thr365Asn
XM_011522368.1:c.1082C>A (CCDC78)	XP_011520670.1:p.Thr361Asn
XM_011522369.1:c.1040C>A (CCDC78)	XP_011520671.1:p.Thr347Asn
XM_011522370.1:c.872C>A (CCDC78)	XP_011520672.1:p.Thr291Asn
XM_011522371.1:c.587C>A (CCDC78)	XP_011520673.1:p.Thr196Asn
XM_006720843.4:c.1028C>A (CCDC78)	XP_006720906.1:p.Thr343Asn
XM_011522358.2:c.1475C>A (CCDC78)	XP_011520660.1:p.Thr492Asn
XM_011522371.2:c.587C>A (CCDC78)	XP_011520673.1:p.Thr196Asn
XM_017022929.1:c.1475C>A (CCDC78)	XP_016878418.1:p.Thr492Asn
XM_017022930.1:c.575C>A (CCDC78)	XP_016878419.1:p.Thr192Asn
XM_024450150.1:c.305C>A (CCDC78)	XP_024305918.1:p.Thr102Asn
XR_001751835.1:n.1814C>A (CCDC78)
XR_001751836.1:n.1793C>A (CCDC78)
XR_001751837.1:n.1571C>A (CCDC78)
XR_001751838.1:n.1917C>A (CCDC78)
XR_001751839.1:n.1379C>A (CCDC78)
NM_001031737.3:c.1028C>A (CCDC78)	NP_001026907.2:p.Thr343Asn
NM_001378030.1:c.1028C>A (CCDC78) MANE Select	NP_001364959.1:p.Thr343Asn
NM_001378031.1:c.953+191C>A (CCDC78)	NP_001364960.1:n.953+191C>A
NM_001378033.1:c.461C>A (CCDC78)	NP_001364962.1:p.Thr154Asn
NR_165382.1:n.1585C>A (CCDC78)
NR_165383.1:n.1231C>A (CCDC78)
NR_165384.1:n.1196C>A (CCDC78)
NR_165385.1:n.1296C>A (CCDC78)
NR_165386.1:n.1363C>A (CCDC78)