Canonical Allele Identifier: CA492830111

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.774142C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724142C>G , CM000678.2:g.724142C>G	GRCh38
NC_000016.9:g.774142C>G , CM000678.1:g.774142C>G	GRCh37
NC_000016.8:g.714143C>G	NCBI36
NG_032932.1:g.7332G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1560G>C (CCDC78)
ENST00000345165.10:c.1017G>C (CCDC78) MANE Select	ENSP00000316851.5:p.Val339=
ENST00000293889.10:c.1017G>C (CCDC78)	ENSP00000293889.6:p.Val339=
ENST00000345165.8:c.563G>C (CCDC78)
ENST00000463539.5:n.1339G>C (CCDC78)
ENST00000466708.5:n.1361G>C (CCDC78)
ENST00000478979.5:n.1495G>C (CCDC78)
ENST00000481804.5:n.1995G>C (CCDC78)
ENST00000482152.1:n.378G>C (CCDC78)
ENST00000482878.5:n.1898G>C (CCDC78)
ENST00000485091.5:n.1170G>C (CCDC78)
ENST00000620831.4:c.-49-38490C>G (MSLN)	ENSP00000482893.1:n.-49-38490C>G
NM_001031737.2:c.1017G>C (CCDC78)	NP_001026907.2:p.Val339=
XM_006720838.1:c.1239G>C (CCDC78)	XP_006720901.1:p.Val413=
XM_006720843.2:c.1017G>C (CCDC78)	XP_006720906.1:p.Val339=
XM_011522356.1:c.1464G>C (CCDC78)	XP_011520658.1:p.Val488=
XM_011522357.1:c.1452G>C (CCDC78)	XP_011520659.1:p.Val484=
XM_011522358.1:c.1464G>C (CCDC78)	XP_011520660.1:p.Val488=
XM_011522359.1:c.1431G>C (CCDC78)	XP_011520661.1:p.Val477=
XM_011522360.1:c.1419G>C (CCDC78)	XP_011520662.1:p.Val473=
XM_011522361.1:c.1464G>C (CCDC78)	XP_011520663.1:p.Val488=
XM_011522362.1:c.1464G>C (CCDC78)	XP_011520664.1:p.Val488=
XM_011522363.1:c.1464G>C (CCDC78)	XP_011520665.1:p.Val488=
XM_011522364.1:c.1464G>C (CCDC78)	XP_011520666.1:p.Val488=
XM_011522365.1:c.1251G>C (CCDC78)	XP_011520667.1:p.Val417=
XM_011522366.1:c.1242G>C (CCDC78)	XP_011520668.1:p.Val414=
XM_011522367.1:c.1083G>C (CCDC78)	XP_011520669.1:p.Val361=
XM_011522368.1:c.1071G>C (CCDC78)	XP_011520670.1:p.Val357=
XM_011522369.1:c.1029G>C (CCDC78)	XP_011520671.1:p.Val343=
XM_011522370.1:c.861G>C (CCDC78)	XP_011520672.1:p.Val287=
XM_011522371.1:c.576G>C (CCDC78)	XP_011520673.1:p.Val192=
XM_006720843.4:c.1017G>C (CCDC78)	XP_006720906.1:p.Val339=
XM_011522358.2:c.1464G>C (CCDC78)	XP_011520660.1:p.Val488=
XM_011522371.2:c.576G>C (CCDC78)	XP_011520673.1:p.Val192=
XM_017022929.1:c.1464G>C (CCDC78)	XP_016878418.1:p.Val488=
XM_017022930.1:c.564G>C (CCDC78)	XP_016878419.1:p.Val188=
XM_024450150.1:c.294G>C (CCDC78)	XP_024305918.1:p.Val98=
XR_001751835.1:n.1803G>C (CCDC78)
XR_001751836.1:n.1782G>C (CCDC78)
XR_001751837.1:n.1560G>C (CCDC78)
XR_001751838.1:n.1906G>C (CCDC78)
XR_001751839.1:n.1368G>C (CCDC78)
NM_001031737.3:c.1017G>C (CCDC78)	NP_001026907.2:p.Val339=
NM_001378030.1:c.1017G>C (CCDC78) MANE Select	NP_001364959.1:p.Val339=
NM_001378031.1:c.953+180G>C (CCDC78)	NP_001364960.1:n.953+180G>C
NM_001378033.1:c.450G>C (CCDC78)	NP_001364962.1:p.Val150=
NR_165382.1:n.1574G>C (CCDC78)
NR_165383.1:n.1220G>C (CCDC78)
NR_165384.1:n.1185G>C (CCDC78)
NR_165385.1:n.1285G>C (CCDC78)
NR_165386.1:n.1352G>C (CCDC78)