Canonical Allele Identifier: CA492830028

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-723859-T-C
• MyVariant Identifiers: chr16:g.773859T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723859T>C , CM000678.2:g.723859T>C	GRCh38
NC_000016.9:g.773859T>C , CM000678.1:g.773859T>C	GRCh37
NC_000016.8:g.713860T>C	NCBI36
NG_032932.1:g.7615A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1674A>G (CCDC78)
ENST00000345165.10:c.1131A>G (CCDC78) MANE Select	ENSP00000316851.5:p.Pro377=
ENST00000293889.10:c.1131A>G (CCDC78)	ENSP00000293889.6:p.Pro377=
ENST00000345165.8:c.677A>G (CCDC78)
ENST00000463539.5:n.1453A>G (CCDC78)
ENST00000466708.5:n.1475A>G (CCDC78)
ENST00000478979.5:n.1778A>G (CCDC78)
ENST00000481804.5:n.2109A>G (CCDC78)
ENST00000482152.1:n.492A>G (CCDC78)
ENST00000482878.5:n.2181A>G (CCDC78)
ENST00000485091.5:n.1284A>G (CCDC78)
ENST00000620831.4:c.-49-38773T>C (MSLN)	ENSP00000482893.1:n.-49-38773T>C
NM_001031737.2:c.1131A>G (CCDC78)	NP_001026907.2:p.Pro377=
XM_006720838.1:c.1353A>G (CCDC78)	XP_006720901.1:p.Pro451=
XM_006720843.2:c.1131A>G (CCDC78)	XP_006720906.1:p.Pro377=
XM_011522356.1:c.1578A>G (CCDC78)	XP_011520658.1:p.Pro526=
XM_011522357.1:c.1566A>G (CCDC78)	XP_011520659.1:p.Pro522=
XM_011522358.1:c.1578A>G (CCDC78)	XP_011520660.1:p.Pro526=
XM_011522359.1:c.1545A>G (CCDC78)	XP_011520661.1:p.Pro515=
XM_011522360.1:c.1533A>G (CCDC78)	XP_011520662.1:p.Pro511=
XM_011522361.1:c.1578A>G (CCDC78)	XP_011520663.1:p.Pro526=
XM_011522362.1:c.1578A>G (CCDC78)	XP_011520664.1:p.Pro526=
XM_011522363.1:c.1578A>G (CCDC78)	XP_011520665.1:p.Pro526=
XM_011522364.1:c.1578A>G (CCDC78)	XP_011520666.1:p.Pro526=
XM_011522365.1:c.1365A>G (CCDC78)	XP_011520667.1:p.Pro455=
XM_011522366.1:c.1356A>G (CCDC78)	XP_011520668.1:p.Pro452=
XM_011522367.1:c.1197A>G (CCDC78)	XP_011520669.1:p.Pro399=
XM_011522368.1:c.1185A>G (CCDC78)	XP_011520670.1:p.Pro395=
XM_011522369.1:c.1143A>G (CCDC78)	XP_011520671.1:p.Pro381=
XM_011522370.1:c.975A>G (CCDC78)	XP_011520672.1:p.Pro325=
XM_011522371.1:c.690A>G (CCDC78)	XP_011520673.1:p.Pro230=
XM_006720843.4:c.1131A>G (CCDC78)	XP_006720906.1:p.Pro377=
XM_011522358.2:c.1578A>G (CCDC78)	XP_011520660.1:p.Pro526=
XM_011522371.2:c.690A>G (CCDC78)	XP_011520673.1:p.Pro230=
XM_017022929.1:c.1578A>G (CCDC78)	XP_016878418.1:p.Pro526=
XM_017022930.1:c.678A>G (CCDC78)	XP_016878419.1:p.Pro226=
XM_017022931.1:c.-123A>G (CCDC78)	XP_016878420.1:n.-123A>G
XM_024450150.1:c.408A>G (CCDC78)	XP_024305918.1:p.Pro136=
XR_001751835.1:n.1917A>G (CCDC78)
XR_001751836.1:n.1896A>G (CCDC78)
XR_001751837.1:n.1674A>G (CCDC78)
XR_001751838.1:n.2020A>G (CCDC78)
XR_001751839.1:n.1482A>G (CCDC78)
NM_001031737.3:c.1131A>G (CCDC78)	NP_001026907.2:p.Pro377=
NM_001378030.1:c.1131A>G (CCDC78) MANE Select	NP_001364959.1:p.Pro377=
NM_001378031.1:c.953+463A>G (CCDC78)	NP_001364960.1:n.953+463A>G
NM_001378033.1:c.564A>G (CCDC78)	NP_001364962.1:p.Pro188=
NR_165382.1:n.1688A>G (CCDC78)
NR_165383.1:n.1334A>G (CCDC78)
NR_165384.1:n.1299A>G (CCDC78)
NR_165385.1:n.1399A>G (CCDC78)
NR_165386.1:n.1466A>G (CCDC78)