Canonical Allele Identifier: CA492830042

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-723877-C-T
• MyVariant Identifiers: chr16:g.773877C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723877C>T , CM000678.2:g.723877C>T	GRCh38
NC_000016.9:g.773877C>T , CM000678.1:g.773877C>T	GRCh37
NC_000016.8:g.713878C>T	NCBI36
NG_032932.1:g.7597G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1656G>A (CCDC78)
ENST00000345165.10:c.1113G>A (CCDC78) MANE Select	ENSP00000316851.5:p.Gln371=
ENST00000293889.10:c.1113G>A (CCDC78)	ENSP00000293889.6:p.Gln371=
ENST00000345165.8:c.659G>A (CCDC78)
ENST00000463539.5:n.1435G>A (CCDC78)
ENST00000466708.5:n.1457G>A (CCDC78)
ENST00000478979.5:n.1760G>A (CCDC78)
ENST00000481804.5:n.2091G>A (CCDC78)
ENST00000482152.1:n.474G>A (CCDC78)
ENST00000482878.5:n.2163G>A (CCDC78)
ENST00000485091.5:n.1266G>A (CCDC78)
ENST00000620831.4:c.-49-38755C>T (MSLN)	ENSP00000482893.1:n.-49-38755C>T
NM_001031737.2:c.1113G>A (CCDC78)	NP_001026907.2:p.Gln371=
XM_006720838.1:c.1335G>A (CCDC78)	XP_006720901.1:p.Gln445=
XM_006720843.2:c.1113G>A (CCDC78)	XP_006720906.1:p.Gln371=
XM_011522356.1:c.1560G>A (CCDC78)	XP_011520658.1:p.Gln520=
XM_011522357.1:c.1548G>A (CCDC78)	XP_011520659.1:p.Gln516=
XM_011522358.1:c.1560G>A (CCDC78)	XP_011520660.1:p.Gln520=
XM_011522359.1:c.1527G>A (CCDC78)	XP_011520661.1:p.Gln509=
XM_011522360.1:c.1515G>A (CCDC78)	XP_011520662.1:p.Gln505=
XM_011522361.1:c.1560G>A (CCDC78)	XP_011520663.1:p.Gln520=
XM_011522362.1:c.1560G>A (CCDC78)	XP_011520664.1:p.Gln520=
XM_011522363.1:c.1560G>A (CCDC78)	XP_011520665.1:p.Gln520=
XM_011522364.1:c.1560G>A (CCDC78)	XP_011520666.1:p.Gln520=
XM_011522365.1:c.1347G>A (CCDC78)	XP_011520667.1:p.Gln449=
XM_011522366.1:c.1338G>A (CCDC78)	XP_011520668.1:p.Gln446=
XM_011522367.1:c.1179G>A (CCDC78)	XP_011520669.1:p.Gln393=
XM_011522368.1:c.1167G>A (CCDC78)	XP_011520670.1:p.Gln389=
XM_011522369.1:c.1125G>A (CCDC78)	XP_011520671.1:p.Gln375=
XM_011522370.1:c.957G>A (CCDC78)	XP_011520672.1:p.Gln319=
XM_011522371.1:c.672G>A (CCDC78)	XP_011520673.1:p.Gln224=
XM_006720843.4:c.1113G>A (CCDC78)	XP_006720906.1:p.Gln371=
XM_011522358.2:c.1560G>A (CCDC78)	XP_011520660.1:p.Gln520=
XM_011522371.2:c.672G>A (CCDC78)	XP_011520673.1:p.Gln224=
XM_017022929.1:c.1560G>A (CCDC78)	XP_016878418.1:p.Gln520=
XM_017022930.1:c.660G>A (CCDC78)	XP_016878419.1:p.Gln220=
XM_017022931.1:c.-141G>A (CCDC78)	XP_016878420.1:n.-141G>A
XM_024450150.1:c.390G>A (CCDC78)	XP_024305918.1:p.Gln130=
XR_001751835.1:n.1899G>A (CCDC78)
XR_001751836.1:n.1878G>A (CCDC78)
XR_001751837.1:n.1656G>A (CCDC78)
XR_001751838.1:n.2002G>A (CCDC78)
XR_001751839.1:n.1464G>A (CCDC78)
NM_001031737.3:c.1113G>A (CCDC78)	NP_001026907.2:p.Gln371=
NM_001378030.1:c.1113G>A (CCDC78) MANE Select	NP_001364959.1:p.Gln371=
NM_001378031.1:c.953+445G>A (CCDC78)	NP_001364960.1:n.953+445G>A
NM_001378033.1:c.546G>A (CCDC78)	NP_001364962.1:p.Gln182=
NR_165382.1:n.1670G>A (CCDC78)
NR_165383.1:n.1316G>A (CCDC78)
NR_165384.1:n.1281G>A (CCDC78)
NR_165385.1:n.1381G>A (CCDC78)
NR_165386.1:n.1448G>A (CCDC78)