Canonical Allele Identifier: CA492830094

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.774121G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724121G>A , CM000678.2:g.724121G>A	GRCh38
NC_000016.9:g.774121G>A , CM000678.1:g.774121G>A	GRCh37
NC_000016.8:g.714122G>A	NCBI36
NG_032932.1:g.7353C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1581C>T (CCDC78)
ENST00000345165.10:c.1038C>T (CCDC78) MANE Select	ENSP00000316851.5:p.Ser346=
ENST00000293889.10:c.1038C>T (CCDC78)	ENSP00000293889.6:p.Ser346=
ENST00000345165.8:c.584C>T (CCDC78)
ENST00000463539.5:n.1360C>T (CCDC78)
ENST00000466708.5:n.1382C>T (CCDC78)
ENST00000478979.5:n.1516C>T (CCDC78)
ENST00000481804.5:n.2016C>T (CCDC78)
ENST00000482152.1:n.399C>T (CCDC78)
ENST00000482878.5:n.1919C>T (CCDC78)
ENST00000485091.5:n.1191C>T (CCDC78)
ENST00000620831.4:c.-49-38511G>A (MSLN)	ENSP00000482893.1:n.-49-38511G>A
NM_001031737.2:c.1038C>T (CCDC78)	NP_001026907.2:p.Ser346=
XM_006720838.1:c.1260C>T (CCDC78)	XP_006720901.1:p.Ser420=
XM_006720843.2:c.1038C>T (CCDC78)	XP_006720906.1:p.Ser346=
XM_011522356.1:c.1485C>T (CCDC78)	XP_011520658.1:p.Ser495=
XM_011522357.1:c.1473C>T (CCDC78)	XP_011520659.1:p.Ser491=
XM_011522358.1:c.1485C>T (CCDC78)	XP_011520660.1:p.Ser495=
XM_011522359.1:c.1452C>T (CCDC78)	XP_011520661.1:p.Ser484=
XM_011522360.1:c.1440C>T (CCDC78)	XP_011520662.1:p.Ser480=
XM_011522361.1:c.1485C>T (CCDC78)	XP_011520663.1:p.Ser495=
XM_011522362.1:c.1485C>T (CCDC78)	XP_011520664.1:p.Ser495=
XM_011522363.1:c.1485C>T (CCDC78)	XP_011520665.1:p.Ser495=
XM_011522364.1:c.1485C>T (CCDC78)	XP_011520666.1:p.Ser495=
XM_011522365.1:c.1272C>T (CCDC78)	XP_011520667.1:p.Ser424=
XM_011522366.1:c.1263C>T (CCDC78)	XP_011520668.1:p.Ser421=
XM_011522367.1:c.1104C>T (CCDC78)	XP_011520669.1:p.Ser368=
XM_011522368.1:c.1092C>T (CCDC78)	XP_011520670.1:p.Ser364=
XM_011522369.1:c.1050C>T (CCDC78)	XP_011520671.1:p.Ser350=
XM_011522370.1:c.882C>T (CCDC78)	XP_011520672.1:p.Ser294=
XM_011522371.1:c.597C>T (CCDC78)	XP_011520673.1:p.Ser199=
XM_006720843.4:c.1038C>T (CCDC78)	XP_006720906.1:p.Ser346=
XM_011522358.2:c.1485C>T (CCDC78)	XP_011520660.1:p.Ser495=
XM_011522371.2:c.597C>T (CCDC78)	XP_011520673.1:p.Ser199=
XM_017022929.1:c.1485C>T (CCDC78)	XP_016878418.1:p.Ser495=
XM_017022930.1:c.585C>T (CCDC78)	XP_016878419.1:p.Ser195=
XM_024450150.1:c.315C>T (CCDC78)	XP_024305918.1:p.Ser105=
XR_001751835.1:n.1824C>T (CCDC78)
XR_001751836.1:n.1803C>T (CCDC78)
XR_001751837.1:n.1581C>T (CCDC78)
XR_001751838.1:n.1927C>T (CCDC78)
XR_001751839.1:n.1389C>T (CCDC78)
NM_001031737.3:c.1038C>T (CCDC78)	NP_001026907.2:p.Ser346=
NM_001378030.1:c.1038C>T (CCDC78) MANE Select	NP_001364959.1:p.Ser346=
NM_001378031.1:c.953+201C>T (CCDC78)	NP_001364960.1:n.953+201C>T
NM_001378033.1:c.471C>T (CCDC78)	NP_001364962.1:p.Ser157=
NR_165382.1:n.1595C>T (CCDC78)
NR_165383.1:n.1241C>T (CCDC78)
NR_165384.1:n.1206C>T (CCDC78)
NR_165385.1:n.1306C>T (CCDC78)
NR_165386.1:n.1373C>T (CCDC78)