Canonical Allele Identifier: CA2201211366

Gene: CCDC78 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723925A= , CM000678.2:g.723925A=	GRCh38
NC_000016.9:g.773925A= , CM000678.1:g.773925A=	GRCh37
NC_000016.8:g.713926A=	NCBI36
NG_032932.1:g.7549T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1608T= (CCDC78)
ENST00000345165.10:c.1065T= (CCDC78) MANE Select	ENSP00000316851.5:p.Pro355=
ENST00000293889.10:c.1065T= (CCDC78)	ENSP00000293889.6:p.Pro355=
ENST00000345165.8:c.611T= (CCDC78)
ENST00000463539.5:n.1387T= (CCDC78)
ENST00000466708.5:n.1409T= (CCDC78)
ENST00000478979.5:n.1712T= (CCDC78)
ENST00000481804.5:n.2043T= (CCDC78)
ENST00000482152.1:n.426T= (CCDC78)
ENST00000482878.5:n.2115T= (CCDC78)
ENST00000485091.5:n.1218T= (CCDC78)
ENST00000620831.4:c.-49-38707A= (MSLN)	ENSP00000482893.1:n.-49-38707A=
NM_001031737.2:c.1065T= (CCDC78)	NP_001026907.2:p.Pro355=
XM_006720838.1:c.1287T= (CCDC78)	XP_006720901.1:p.Pro429=
XM_006720843.2:c.1065T= (CCDC78)	XP_006720906.1:p.Pro355=
XM_011522356.1:c.1512T= (CCDC78)	XP_011520658.1:p.Pro504=
XM_011522357.1:c.1500T= (CCDC78)	XP_011520659.1:p.Pro500=
XM_011522358.1:c.1512T= (CCDC78)	XP_011520660.1:p.Pro504=
XM_011522359.1:c.1479T= (CCDC78)	XP_011520661.1:p.Pro493=
XM_011522360.1:c.1467T= (CCDC78)	XP_011520662.1:p.Pro489=
XM_011522361.1:c.1512T= (CCDC78)	XP_011520663.1:p.Pro504=
XM_011522362.1:c.1512T= (CCDC78)	XP_011520664.1:p.Pro504=
XM_011522363.1:c.1512T= (CCDC78)	XP_011520665.1:p.Pro504=
XM_011522364.1:c.1512T= (CCDC78)	XP_011520666.1:p.Pro504=
XM_011522365.1:c.1299T= (CCDC78)	XP_011520667.1:p.Pro433=
XM_011522366.1:c.1290T= (CCDC78)	XP_011520668.1:p.Pro430=
XM_011522367.1:c.1131T= (CCDC78)	XP_011520669.1:p.Pro377=
XM_011522368.1:c.1119T= (CCDC78)	XP_011520670.1:p.Pro373=
XM_011522369.1:c.1077T= (CCDC78)	XP_011520671.1:p.Pro359=
XM_011522370.1:c.909T= (CCDC78)	XP_011520672.1:p.Pro303=
XM_011522371.1:c.624T= (CCDC78)	XP_011520673.1:p.Pro208=
XM_006720843.4:c.1065T= (CCDC78)	XP_006720906.1:p.Pro355=
XM_011522358.2:c.1512T= (CCDC78)	XP_011520660.1:p.Pro504=
XM_011522371.2:c.624T= (CCDC78)	XP_011520673.1:p.Pro208=
XM_017022929.1:c.1512T= (CCDC78)	XP_016878418.1:p.Pro504=
XM_017022930.1:c.612T= (CCDC78)	XP_016878419.1:p.Pro204=
XM_017022931.1:c.-189T= (CCDC78)	XP_016878420.1:n.-189T=
XM_024450150.1:c.342T= (CCDC78)	XP_024305918.1:p.Pro114=
XR_001751835.1:n.1851T= (CCDC78)
XR_001751836.1:n.1830T= (CCDC78)
XR_001751837.1:n.1608T= (CCDC78)
XR_001751838.1:n.1954T= (CCDC78)
XR_001751839.1:n.1416T= (CCDC78)
NM_001031737.3:c.1065T= (CCDC78)	NP_001026907.2:p.Pro355=
NM_001378030.1:c.1065T= (CCDC78) MANE Select	NP_001364959.1:p.Pro355=
NM_001378031.1:c.953+397T= (CCDC78)	NP_001364960.1:n.953+397T=
NM_001378033.1:c.498T= (CCDC78)	NP_001364962.1:p.Pro166=
NR_165382.1:n.1622T= (CCDC78)
NR_165383.1:n.1268T= (CCDC78)
NR_165384.1:n.1233T= (CCDC78)
NR_165385.1:n.1333T= (CCDC78)
NR_165386.1:n.1400T= (CCDC78)