Canonical Allele Identifier: CA276519705

Gene: CCDC78 MSLN

Linked Data

• dbSNP Id: rs933251369
• MyVariant Identifiers: chr16:g.773911G>A (hg19) ; chr16:g.723911G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723911G>A , CM000678.2:g.723911G>A	GRCh38
NC_000016.9:g.773911G>A , CM000678.1:g.773911G>A	GRCh37
NC_000016.8:g.713912G>A	NCBI36
NG_032932.1:g.7563C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1622C>T (CCDC78)
ENST00000345165.10:c.1079C>T (CCDC78) MANE Select	ENSP00000316851.5:p.Ser360Leu
ENST00000293889.10:c.1079C>T (CCDC78)	ENSP00000293889.6:p.Ser360Leu
ENST00000345165.8:c.625C>T (CCDC78)
ENST00000463539.5:n.1401C>T (CCDC78)
ENST00000466708.5:n.1423C>T (CCDC78)
ENST00000478979.5:n.1726C>T (CCDC78)
ENST00000481804.5:n.2057C>T (CCDC78)
ENST00000482152.1:n.440C>T (CCDC78)
ENST00000482878.5:n.2129C>T (CCDC78)
ENST00000485091.5:n.1232C>T (CCDC78)
ENST00000620831.4:c.-49-38721G>A (MSLN)	ENSP00000482893.1:n.-49-38721G>A
NM_001031737.2:c.1079C>T (CCDC78)	NP_001026907.2:p.Ser360Leu
XM_006720838.1:c.1301C>T (CCDC78)	XP_006720901.1:p.Ser434Leu
XM_006720843.2:c.1079C>T (CCDC78)	XP_006720906.1:p.Ser360Leu
XM_011522356.1:c.1526C>T (CCDC78)	XP_011520658.1:p.Ser509Leu
XM_011522357.1:c.1514C>T (CCDC78)	XP_011520659.1:p.Ser505Leu
XM_011522358.1:c.1526C>T (CCDC78)	XP_011520660.1:p.Ser509Leu
XM_011522359.1:c.1493C>T (CCDC78)	XP_011520661.1:p.Ser498Leu
XM_011522360.1:c.1481C>T (CCDC78)	XP_011520662.1:p.Ser494Leu
XM_011522361.1:c.1526C>T (CCDC78)	XP_011520663.1:p.Ser509Leu
XM_011522362.1:c.1526C>T (CCDC78)	XP_011520664.1:p.Ser509Leu
XM_011522363.1:c.1526C>T (CCDC78)	XP_011520665.1:p.Ser509Leu
XM_011522364.1:c.1526C>T (CCDC78)	XP_011520666.1:p.Ser509Leu
XM_011522365.1:c.1313C>T (CCDC78)	XP_011520667.1:p.Ser438Leu
XM_011522366.1:c.1304C>T (CCDC78)	XP_011520668.1:p.Ser435Leu
XM_011522367.1:c.1145C>T (CCDC78)	XP_011520669.1:p.Ser382Leu
XM_011522368.1:c.1133C>T (CCDC78)	XP_011520670.1:p.Ser378Leu
XM_011522369.1:c.1091C>T (CCDC78)	XP_011520671.1:p.Ser364Leu
XM_011522370.1:c.923C>T (CCDC78)	XP_011520672.1:p.Ser308Leu
XM_011522371.1:c.638C>T (CCDC78)	XP_011520673.1:p.Ser213Leu
XM_006720843.4:c.1079C>T (CCDC78)	XP_006720906.1:p.Ser360Leu
XM_011522358.2:c.1526C>T (CCDC78)	XP_011520660.1:p.Ser509Leu
XM_011522371.2:c.638C>T (CCDC78)	XP_011520673.1:p.Ser213Leu
XM_017022929.1:c.1526C>T (CCDC78)	XP_016878418.1:p.Ser509Leu
XM_017022930.1:c.626C>T (CCDC78)	XP_016878419.1:p.Ser209Leu
XM_017022931.1:c.-175C>T (CCDC78)	XP_016878420.1:n.-175C>T
XM_024450150.1:c.356C>T (CCDC78)	XP_024305918.1:p.Ser119Leu
XR_001751835.1:n.1865C>T (CCDC78)
XR_001751836.1:n.1844C>T (CCDC78)
XR_001751837.1:n.1622C>T (CCDC78)
XR_001751838.1:n.1968C>T (CCDC78)
XR_001751839.1:n.1430C>T (CCDC78)
NM_001031737.3:c.1079C>T (CCDC78)	NP_001026907.2:p.Ser360Leu
NM_001378030.1:c.1079C>T (CCDC78) MANE Select	NP_001364959.1:p.Ser360Leu
NM_001378031.1:c.953+411C>T (CCDC78)	NP_001364960.1:n.953+411C>T
NM_001378033.1:c.512C>T (CCDC78)	NP_001364962.1:p.Ser171Leu
NR_165382.1:n.1636C>T (CCDC78)
NR_165383.1:n.1282C>T (CCDC78)
NR_165384.1:n.1247C>T (CCDC78)
NR_165385.1:n.1347C>T (CCDC78)
NR_165386.1:n.1414C>T (CCDC78)