Canonical Allele Identifier: CA394098399

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.773898C>G (hg19) ; chr16:g.723898C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723898C>G , CM000678.2:g.723898C>G	GRCh38
NC_000016.9:g.773898C>G , CM000678.1:g.773898C>G	GRCh37
NC_000016.8:g.713899C>G	NCBI36
NG_032932.1:g.7576G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1635G>C (CCDC78)
ENST00000345165.10:c.1092G>C (CCDC78) MANE Select	ENSP00000316851.5:p.Lys364Asn
ENST00000293889.10:c.1092G>C (CCDC78)	ENSP00000293889.6:p.Lys364Asn
ENST00000345165.8:c.638G>C (CCDC78)
ENST00000463539.5:n.1414G>C (CCDC78)
ENST00000466708.5:n.1436G>C (CCDC78)
ENST00000478979.5:n.1739G>C (CCDC78)
ENST00000481804.5:n.2070G>C (CCDC78)
ENST00000482152.1:n.453G>C (CCDC78)
ENST00000482878.5:n.2142G>C (CCDC78)
ENST00000485091.5:n.1245G>C (CCDC78)
ENST00000620831.4:c.-49-38734C>G (MSLN)	ENSP00000482893.1:n.-49-38734C>G
NM_001031737.2:c.1092G>C (CCDC78)	NP_001026907.2:p.Lys364Asn
XM_006720838.1:c.1314G>C (CCDC78)	XP_006720901.1:p.Lys438Asn
XM_006720843.2:c.1092G>C (CCDC78)	XP_006720906.1:p.Lys364Asn
XM_011522356.1:c.1539G>C (CCDC78)	XP_011520658.1:p.Lys513Asn
XM_011522357.1:c.1527G>C (CCDC78)	XP_011520659.1:p.Lys509Asn
XM_011522358.1:c.1539G>C (CCDC78)	XP_011520660.1:p.Lys513Asn
XM_011522359.1:c.1506G>C (CCDC78)	XP_011520661.1:p.Lys502Asn
XM_011522360.1:c.1494G>C (CCDC78)	XP_011520662.1:p.Lys498Asn
XM_011522361.1:c.1539G>C (CCDC78)	XP_011520663.1:p.Lys513Asn
XM_011522362.1:c.1539G>C (CCDC78)	XP_011520664.1:p.Lys513Asn
XM_011522363.1:c.1539G>C (CCDC78)	XP_011520665.1:p.Lys513Asn
XM_011522364.1:c.1539G>C (CCDC78)	XP_011520666.1:p.Lys513Asn
XM_011522365.1:c.1326G>C (CCDC78)	XP_011520667.1:p.Lys442Asn
XM_011522366.1:c.1317G>C (CCDC78)	XP_011520668.1:p.Lys439Asn
XM_011522367.1:c.1158G>C (CCDC78)	XP_011520669.1:p.Lys386Asn
XM_011522368.1:c.1146G>C (CCDC78)	XP_011520670.1:p.Lys382Asn
XM_011522369.1:c.1104G>C (CCDC78)	XP_011520671.1:p.Lys368Asn
XM_011522370.1:c.936G>C (CCDC78)	XP_011520672.1:p.Lys312Asn
XM_011522371.1:c.651G>C (CCDC78)	XP_011520673.1:p.Lys217Asn
XM_006720843.4:c.1092G>C (CCDC78)	XP_006720906.1:p.Lys364Asn
XM_011522358.2:c.1539G>C (CCDC78)	XP_011520660.1:p.Lys513Asn
XM_011522371.2:c.651G>C (CCDC78)	XP_011520673.1:p.Lys217Asn
XM_017022929.1:c.1539G>C (CCDC78)	XP_016878418.1:p.Lys513Asn
XM_017022930.1:c.639G>C (CCDC78)	XP_016878419.1:p.Lys213Asn
XM_017022931.1:c.-162G>C (CCDC78)	XP_016878420.1:n.-162G>C
XM_024450150.1:c.369G>C (CCDC78)	XP_024305918.1:p.Lys123Asn
XR_001751835.1:n.1878G>C (CCDC78)
XR_001751836.1:n.1857G>C (CCDC78)
XR_001751837.1:n.1635G>C (CCDC78)
XR_001751838.1:n.1981G>C (CCDC78)
XR_001751839.1:n.1443G>C (CCDC78)
NM_001031737.3:c.1092G>C (CCDC78)	NP_001026907.2:p.Lys364Asn
NM_001378030.1:c.1092G>C (CCDC78) MANE Select	NP_001364959.1:p.Lys364Asn
NM_001378031.1:c.953+424G>C (CCDC78)	NP_001364960.1:n.953+424G>C
NM_001378033.1:c.525G>C (CCDC78)	NP_001364962.1:p.Lys175Asn
NR_165382.1:n.1649G>C (CCDC78)
NR_165383.1:n.1295G>C (CCDC78)
NR_165384.1:n.1260G>C (CCDC78)
NR_165385.1:n.1360G>C (CCDC78)
NR_165386.1:n.1427G>C (CCDC78)