Canonical Allele Identifier: CA394103163

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.775261A>T (hg19) ; chr16:g.725261A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.725261A>T , CM000678.2:g.725261A>T	GRCh38
NC_000016.9:g.775261A>T , CM000678.1:g.775261A>T	GRCh37
NC_000016.8:g.715262A>T	NCBI36
NG_032932.1:g.6213T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423653.6:n.513T>A (CCDC78)
ENST00000682391.1:n.557T>A (CCDC78)
ENST00000345165.10:c.468T>A (CCDC78) MANE Select	ENSP00000316851.5:p.Asn156Lys
ENST00000293889.10:c.468T>A (CCDC78)	ENSP00000293889.6:p.Asn156Lys
ENST00000345165.8:c.14T>A (CCDC78)
ENST00000423653.5:c.15T>A (CCDC78)	ENSP00000458590.1:p.Asn5Lys
ENST00000439619.6:n.545T>A (CCDC78)
ENST00000460023.5:n.435T>A (CCDC78)
ENST00000463539.5:n.531T>A (CCDC78)
ENST00000466708.5:n.641T>A (CCDC78)
ENST00000471861.5:n.574T>A (CCDC78)
ENST00000474647.1:n.368T>A (CCDC78)
ENST00000478979.5:n.376T>A (CCDC78)
ENST00000481804.5:n.876T>A (CCDC78)
ENST00000482878.5:n.779T>A (CCDC78)
ENST00000485091.5:n.530T>A (CCDC78)
ENST00000538176.5:n.538T>A (CCDC78)
ENST00000544996.1:n.274T>A (CCDC78)
ENST00000620831.4:c.-49-37371A>T (MSLN)	ENSP00000482893.1:n.-49-37371A>T
NM_001031737.2:c.468T>A (CCDC78)	NP_001026907.2:p.Asn156Lys
XM_005255106.3:c.435T>A (CCDC78)	XP_005255163.1:p.Asn145Lys
XM_006720838.1:c.690T>A (CCDC78)	XP_006720901.1:p.Asn230Lys
XM_006720843.2:c.468T>A (CCDC78)	XP_006720906.1:p.Asn156Lys
XM_011522356.1:c.903T>A (CCDC78)	XP_011520658.1:p.Asn301Lys
XM_011522357.1:c.903T>A (CCDC78)	XP_011520659.1:p.Asn301Lys
XM_011522358.1:c.903T>A (CCDC78)	XP_011520660.1:p.Asn301Lys
XM_011522359.1:c.870T>A (CCDC78)	XP_011520661.1:p.Asn290Lys
XM_011522360.1:c.870T>A (CCDC78)	XP_011520662.1:p.Asn290Lys
XM_011522361.1:c.903T>A (CCDC78)	XP_011520663.1:p.Asn301Lys
XM_011522362.1:c.903T>A (CCDC78)	XP_011520664.1:p.Asn301Lys
XM_011522363.1:c.903T>A (CCDC78)	XP_011520665.1:p.Asn301Lys
XM_011522364.1:c.903T>A (CCDC78)	XP_011520666.1:p.Asn301Lys
XM_011522365.1:c.690T>A (CCDC78)	XP_011520667.1:p.Asn230Lys
XM_011522366.1:c.681T>A (CCDC78)	XP_011520668.1:p.Asn227Lys
XM_011522367.1:c.522T>A (CCDC78)	XP_011520669.1:p.Asn174Lys
XM_011522368.1:c.522T>A (CCDC78)	XP_011520670.1:p.Asn174Lys
XM_011522369.1:c.468T>A (CCDC78)	XP_011520671.1:p.Asn156Lys
XM_011522370.1:c.300T>A (CCDC78)	XP_011520672.1:p.Asn100Lys
XM_011522371.1:c.15T>A (CCDC78)	XP_011520673.1:p.Asn5Lys
XM_006720843.4:c.468T>A (CCDC78)	XP_006720906.1:p.Asn156Lys
XM_011522358.2:c.903T>A (CCDC78)	XP_011520660.1:p.Asn301Lys
XM_011522371.2:c.15T>A (CCDC78)	XP_011520673.1:p.Asn5Lys
XM_017022929.1:c.903T>A (CCDC78)	XP_016878418.1:p.Asn301Lys
XM_017022930.1:c.15T>A (CCDC78)	XP_016878419.1:p.Asn5Lys
XR_001751835.1:n.992T>A (CCDC78)
XR_001751836.1:n.779T>A (CCDC78)
XR_001751837.1:n.557T>A (CCDC78)
XR_001751838.1:n.903T>A (CCDC78)
XR_001751839.1:n.557T>A (CCDC78)
NM_001031737.3:c.468T>A (CCDC78)	NP_001026907.2:p.Asn156Lys
NM_001378030.1:c.468T>A (CCDC78) MANE Select	NP_001364959.1:p.Asn156Lys
NM_001378031.1:c.468T>A (CCDC78)	NP_001364960.1:p.Asn156Lys
NM_001378033.1:c.15T>A (CCDC78)	NP_001364962.1:p.Asn5Lys
NR_165382.1:n.766T>A (CCDC78)
NR_165383.1:n.500T>A (CCDC78)
NR_165384.1:n.467T>A (CCDC78)
NR_165385.1:n.544T>A (CCDC78)
NR_165386.1:n.544T>A (CCDC78)