Canonical Allele Identifier: CA394098833

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.774129C>T (hg19) ; chr16:g.724129C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724129C>T , CM000678.2:g.724129C>T	GRCh38
NC_000016.9:g.774129C>T , CM000678.1:g.774129C>T	GRCh37
NC_000016.8:g.714130C>T	NCBI36
NG_032932.1:g.7345G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1573G>A (CCDC78)
ENST00000345165.10:c.1030G>A (CCDC78) MANE Select	ENSP00000316851.5:p.Asp344Asn
ENST00000293889.10:c.1030G>A (CCDC78)	ENSP00000293889.6:p.Asp344Asn
ENST00000345165.8:c.576G>A (CCDC78)
ENST00000463539.5:n.1352G>A (CCDC78)
ENST00000466708.5:n.1374G>A (CCDC78)
ENST00000478979.5:n.1508G>A (CCDC78)
ENST00000481804.5:n.2008G>A (CCDC78)
ENST00000482152.1:n.391G>A (CCDC78)
ENST00000482878.5:n.1911G>A (CCDC78)
ENST00000485091.5:n.1183G>A (CCDC78)
ENST00000620831.4:c.-49-38503C>T (MSLN)	ENSP00000482893.1:n.-49-38503C>T
NM_001031737.2:c.1030G>A (CCDC78)	NP_001026907.2:p.Asp344Asn
XM_006720838.1:c.1252G>A (CCDC78)	XP_006720901.1:p.Asp418Asn
XM_006720843.2:c.1030G>A (CCDC78)	XP_006720906.1:p.Asp344Asn
XM_011522356.1:c.1477G>A (CCDC78)	XP_011520658.1:p.Asp493Asn
XM_011522357.1:c.1465G>A (CCDC78)	XP_011520659.1:p.Asp489Asn
XM_011522358.1:c.1477G>A (CCDC78)	XP_011520660.1:p.Asp493Asn
XM_011522359.1:c.1444G>A (CCDC78)	XP_011520661.1:p.Asp482Asn
XM_011522360.1:c.1432G>A (CCDC78)	XP_011520662.1:p.Asp478Asn
XM_011522361.1:c.1477G>A (CCDC78)	XP_011520663.1:p.Asp493Asn
XM_011522362.1:c.1477G>A (CCDC78)	XP_011520664.1:p.Asp493Asn
XM_011522363.1:c.1477G>A (CCDC78)	XP_011520665.1:p.Asp493Asn
XM_011522364.1:c.1477G>A (CCDC78)	XP_011520666.1:p.Asp493Asn
XM_011522365.1:c.1264G>A (CCDC78)	XP_011520667.1:p.Asp422Asn
XM_011522366.1:c.1255G>A (CCDC78)	XP_011520668.1:p.Asp419Asn
XM_011522367.1:c.1096G>A (CCDC78)	XP_011520669.1:p.Asp366Asn
XM_011522368.1:c.1084G>A (CCDC78)	XP_011520670.1:p.Asp362Asn
XM_011522369.1:c.1042G>A (CCDC78)	XP_011520671.1:p.Asp348Asn
XM_011522370.1:c.874G>A (CCDC78)	XP_011520672.1:p.Asp292Asn
XM_011522371.1:c.589G>A (CCDC78)	XP_011520673.1:p.Asp197Asn
XM_006720843.4:c.1030G>A (CCDC78)	XP_006720906.1:p.Asp344Asn
XM_011522358.2:c.1477G>A (CCDC78)	XP_011520660.1:p.Asp493Asn
XM_011522371.2:c.589G>A (CCDC78)	XP_011520673.1:p.Asp197Asn
XM_017022929.1:c.1477G>A (CCDC78)	XP_016878418.1:p.Asp493Asn
XM_017022930.1:c.577G>A (CCDC78)	XP_016878419.1:p.Asp193Asn
XM_024450150.1:c.307G>A (CCDC78)	XP_024305918.1:p.Asp103Asn
XR_001751835.1:n.1816G>A (CCDC78)
XR_001751836.1:n.1795G>A (CCDC78)
XR_001751837.1:n.1573G>A (CCDC78)
XR_001751838.1:n.1919G>A (CCDC78)
XR_001751839.1:n.1381G>A (CCDC78)
NM_001031737.3:c.1030G>A (CCDC78)	NP_001026907.2:p.Asp344Asn
NM_001378030.1:c.1030G>A (CCDC78) MANE Select	NP_001364959.1:p.Asp344Asn
NM_001378031.1:c.953+193G>A (CCDC78)	NP_001364960.1:n.953+193G>A
NM_001378033.1:c.463G>A (CCDC78)	NP_001364962.1:p.Asp155Asn
NR_165382.1:n.1587G>A (CCDC78)
NR_165383.1:n.1233G>A (CCDC78)
NR_165384.1:n.1198G>A (CCDC78)
NR_165385.1:n.1298G>A (CCDC78)
NR_165386.1:n.1365G>A (CCDC78)