Canonical Allele Identifier: CA394098780

Gene: CCDC78 MSLN

Linked Data

• dbSNP Id: rs1378836403
• gnomAD v2: 16-774123-T-C
• gnomAD v3: 16-724123-T-C
• gnomAD v4: 16-724123-T-C
• MyVariant Identifiers: chr16:g.774123T>C (hg19) ; chr16:g.724123T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724123T>C , CM000678.2:g.724123T>C	GRCh38
NC_000016.9:g.774123T>C , CM000678.1:g.774123T>C	GRCh37
NC_000016.8:g.714124T>C	NCBI36
NG_032932.1:g.7351A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1579A>G (CCDC78)
ENST00000345165.10:c.1036A>G (CCDC78) MANE Select	ENSP00000316851.5:p.Ser346Gly
ENST00000293889.10:c.1036A>G (CCDC78)	ENSP00000293889.6:p.Ser346Gly
ENST00000345165.8:c.582A>G (CCDC78)
ENST00000463539.5:n.1358A>G (CCDC78)
ENST00000466708.5:n.1380A>G (CCDC78)
ENST00000478979.5:n.1514A>G (CCDC78)
ENST00000481804.5:n.2014A>G (CCDC78)
ENST00000482152.1:n.397A>G (CCDC78)
ENST00000482878.5:n.1917A>G (CCDC78)
ENST00000485091.5:n.1189A>G (CCDC78)
ENST00000620831.4:c.-49-38509T>C (MSLN)	ENSP00000482893.1:n.-49-38509T>C
NM_001031737.2:c.1036A>G (CCDC78)	NP_001026907.2:p.Ser346Gly
XM_006720838.1:c.1258A>G (CCDC78)	XP_006720901.1:p.Ser420Gly
XM_006720843.2:c.1036A>G (CCDC78)	XP_006720906.1:p.Ser346Gly
XM_011522356.1:c.1483A>G (CCDC78)	XP_011520658.1:p.Ser495Gly
XM_011522357.1:c.1471A>G (CCDC78)	XP_011520659.1:p.Ser491Gly
XM_011522358.1:c.1483A>G (CCDC78)	XP_011520660.1:p.Ser495Gly
XM_011522359.1:c.1450A>G (CCDC78)	XP_011520661.1:p.Ser484Gly
XM_011522360.1:c.1438A>G (CCDC78)	XP_011520662.1:p.Ser480Gly
XM_011522361.1:c.1483A>G (CCDC78)	XP_011520663.1:p.Ser495Gly
XM_011522362.1:c.1483A>G (CCDC78)	XP_011520664.1:p.Ser495Gly
XM_011522363.1:c.1483A>G (CCDC78)	XP_011520665.1:p.Ser495Gly
XM_011522364.1:c.1483A>G (CCDC78)	XP_011520666.1:p.Ser495Gly
XM_011522365.1:c.1270A>G (CCDC78)	XP_011520667.1:p.Ser424Gly
XM_011522366.1:c.1261A>G (CCDC78)	XP_011520668.1:p.Ser421Gly
XM_011522367.1:c.1102A>G (CCDC78)	XP_011520669.1:p.Ser368Gly
XM_011522368.1:c.1090A>G (CCDC78)	XP_011520670.1:p.Ser364Gly
XM_011522369.1:c.1048A>G (CCDC78)	XP_011520671.1:p.Ser350Gly
XM_011522370.1:c.880A>G (CCDC78)	XP_011520672.1:p.Ser294Gly
XM_011522371.1:c.595A>G (CCDC78)	XP_011520673.1:p.Ser199Gly
XM_006720843.4:c.1036A>G (CCDC78)	XP_006720906.1:p.Ser346Gly
XM_011522358.2:c.1483A>G (CCDC78)	XP_011520660.1:p.Ser495Gly
XM_011522371.2:c.595A>G (CCDC78)	XP_011520673.1:p.Ser199Gly
XM_017022929.1:c.1483A>G (CCDC78)	XP_016878418.1:p.Ser495Gly
XM_017022930.1:c.583A>G (CCDC78)	XP_016878419.1:p.Ser195Gly
XM_024450150.1:c.313A>G (CCDC78)	XP_024305918.1:p.Ser105Gly
XR_001751835.1:n.1822A>G (CCDC78)
XR_001751836.1:n.1801A>G (CCDC78)
XR_001751837.1:n.1579A>G (CCDC78)
XR_001751838.1:n.1925A>G (CCDC78)
XR_001751839.1:n.1387A>G (CCDC78)
NM_001031737.3:c.1036A>G (CCDC78)	NP_001026907.2:p.Ser346Gly
NM_001378030.1:c.1036A>G (CCDC78) MANE Select	NP_001364959.1:p.Ser346Gly
NM_001378031.1:c.953+199A>G (CCDC78)	NP_001364960.1:n.953+199A>G
NM_001378033.1:c.469A>G (CCDC78)	NP_001364962.1:p.Ser157Gly
NR_165382.1:n.1593A>G (CCDC78)
NR_165383.1:n.1239A>G (CCDC78)
NR_165384.1:n.1204A>G (CCDC78)
NR_165385.1:n.1304A>G (CCDC78)
NR_165386.1:n.1371A>G (CCDC78)