Canonical Allele Identifier: CA492830057

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.773897T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723897T>G , CM000678.2:g.723897T>G	GRCh38
NC_000016.9:g.773897T>G , CM000678.1:g.773897T>G	GRCh37
NC_000016.8:g.713898T>G	NCBI36
NG_032932.1:g.7577A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1636A>C (CCDC78)
ENST00000345165.10:c.1093A>C (CCDC78) MANE Select	ENSP00000316851.5:p.Arg365=
ENST00000293889.10:c.1093A>C (CCDC78)	ENSP00000293889.6:p.Arg365=
ENST00000345165.8:c.639A>C (CCDC78)
ENST00000463539.5:n.1415A>C (CCDC78)
ENST00000466708.5:n.1437A>C (CCDC78)
ENST00000478979.5:n.1740A>C (CCDC78)
ENST00000481804.5:n.2071A>C (CCDC78)
ENST00000482152.1:n.454A>C (CCDC78)
ENST00000482878.5:n.2143A>C (CCDC78)
ENST00000485091.5:n.1246A>C (CCDC78)
ENST00000620831.4:c.-49-38735T>G (MSLN)	ENSP00000482893.1:n.-49-38735T>G
NM_001031737.2:c.1093A>C (CCDC78)	NP_001026907.2:p.Arg365=
XM_006720838.1:c.1315A>C (CCDC78)	XP_006720901.1:p.Arg439=
XM_006720843.2:c.1093A>C (CCDC78)	XP_006720906.1:p.Arg365=
XM_011522356.1:c.1540A>C (CCDC78)	XP_011520658.1:p.Arg514=
XM_011522357.1:c.1528A>C (CCDC78)	XP_011520659.1:p.Arg510=
XM_011522358.1:c.1540A>C (CCDC78)	XP_011520660.1:p.Arg514=
XM_011522359.1:c.1507A>C (CCDC78)	XP_011520661.1:p.Arg503=
XM_011522360.1:c.1495A>C (CCDC78)	XP_011520662.1:p.Arg499=
XM_011522361.1:c.1540A>C (CCDC78)	XP_011520663.1:p.Arg514=
XM_011522362.1:c.1540A>C (CCDC78)	XP_011520664.1:p.Arg514=
XM_011522363.1:c.1540A>C (CCDC78)	XP_011520665.1:p.Arg514=
XM_011522364.1:c.1540A>C (CCDC78)	XP_011520666.1:p.Arg514=
XM_011522365.1:c.1327A>C (CCDC78)	XP_011520667.1:p.Arg443=
XM_011522366.1:c.1318A>C (CCDC78)	XP_011520668.1:p.Arg440=
XM_011522367.1:c.1159A>C (CCDC78)	XP_011520669.1:p.Arg387=
XM_011522368.1:c.1147A>C (CCDC78)	XP_011520670.1:p.Arg383=
XM_011522369.1:c.1105A>C (CCDC78)	XP_011520671.1:p.Arg369=
XM_011522370.1:c.937A>C (CCDC78)	XP_011520672.1:p.Arg313=
XM_011522371.1:c.652A>C (CCDC78)	XP_011520673.1:p.Arg218=
XM_006720843.4:c.1093A>C (CCDC78)	XP_006720906.1:p.Arg365=
XM_011522358.2:c.1540A>C (CCDC78)	XP_011520660.1:p.Arg514=
XM_011522371.2:c.652A>C (CCDC78)	XP_011520673.1:p.Arg218=
XM_017022929.1:c.1540A>C (CCDC78)	XP_016878418.1:p.Arg514=
XM_017022930.1:c.640A>C (CCDC78)	XP_016878419.1:p.Arg214=
XM_017022931.1:c.-161A>C (CCDC78)	XP_016878420.1:n.-161A>C
XM_024450150.1:c.370A>C (CCDC78)	XP_024305918.1:p.Arg124=
XR_001751835.1:n.1879A>C (CCDC78)
XR_001751836.1:n.1858A>C (CCDC78)
XR_001751837.1:n.1636A>C (CCDC78)
XR_001751838.1:n.1982A>C (CCDC78)
XR_001751839.1:n.1444A>C (CCDC78)
NM_001031737.3:c.1093A>C (CCDC78)	NP_001026907.2:p.Arg365=
NM_001378030.1:c.1093A>C (CCDC78) MANE Select	NP_001364959.1:p.Arg365=
NM_001378031.1:c.953+425A>C (CCDC78)	NP_001364960.1:n.953+425A>C
NM_001378033.1:c.526A>C (CCDC78)	NP_001364962.1:p.Arg176=
NR_165382.1:n.1650A>C (CCDC78)
NR_165383.1:n.1296A>C (CCDC78)
NR_165384.1:n.1261A>C (CCDC78)
NR_165385.1:n.1361A>C (CCDC78)
NR_165386.1:n.1428A>C (CCDC78)