Canonical Allele Identifier: CA2201211365

Gene: CCDC78 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723924C= , CM000678.2:g.723924C=	GRCh38
NC_000016.9:g.773924C= , CM000678.1:g.773924C=	GRCh37
NC_000016.8:g.713925C=	NCBI36
NG_032932.1:g.7550G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1609G= (CCDC78)
ENST00000345165.10:c.1066G= (CCDC78) MANE Select	ENSP00000316851.5:p.Gly356=
ENST00000293889.10:c.1066G= (CCDC78)	ENSP00000293889.6:p.Gly356=
ENST00000345165.8:c.612G= (CCDC78)
ENST00000463539.5:n.1388G= (CCDC78)
ENST00000466708.5:n.1410G= (CCDC78)
ENST00000478979.5:n.1713G= (CCDC78)
ENST00000481804.5:n.2044G= (CCDC78)
ENST00000482152.1:n.427G= (CCDC78)
ENST00000482878.5:n.2116G= (CCDC78)
ENST00000485091.5:n.1219G= (CCDC78)
ENST00000620831.4:c.-49-38708C= (MSLN)	ENSP00000482893.1:n.-49-38708C=
NM_001031737.2:c.1066G= (CCDC78)	NP_001026907.2:p.Gly356=
XM_006720838.1:c.1288G= (CCDC78)	XP_006720901.1:p.Gly430=
XM_006720843.2:c.1066G= (CCDC78)	XP_006720906.1:p.Gly356=
XM_011522356.1:c.1513G= (CCDC78)	XP_011520658.1:p.Gly505=
XM_011522357.1:c.1501G= (CCDC78)	XP_011520659.1:p.Gly501=
XM_011522358.1:c.1513G= (CCDC78)	XP_011520660.1:p.Gly505=
XM_011522359.1:c.1480G= (CCDC78)	XP_011520661.1:p.Gly494=
XM_011522360.1:c.1468G= (CCDC78)	XP_011520662.1:p.Gly490=
XM_011522361.1:c.1513G= (CCDC78)	XP_011520663.1:p.Gly505=
XM_011522362.1:c.1513G= (CCDC78)	XP_011520664.1:p.Gly505=
XM_011522363.1:c.1513G= (CCDC78)	XP_011520665.1:p.Gly505=
XM_011522364.1:c.1513G= (CCDC78)	XP_011520666.1:p.Gly505=
XM_011522365.1:c.1300G= (CCDC78)	XP_011520667.1:p.Gly434=
XM_011522366.1:c.1291G= (CCDC78)	XP_011520668.1:p.Gly431=
XM_011522367.1:c.1132G= (CCDC78)	XP_011520669.1:p.Gly378=
XM_011522368.1:c.1120G= (CCDC78)	XP_011520670.1:p.Gly374=
XM_011522369.1:c.1078G= (CCDC78)	XP_011520671.1:p.Gly360=
XM_011522370.1:c.910G= (CCDC78)	XP_011520672.1:p.Gly304=
XM_011522371.1:c.625G= (CCDC78)	XP_011520673.1:p.Gly209=
XM_006720843.4:c.1066G= (CCDC78)	XP_006720906.1:p.Gly356=
XM_011522358.2:c.1513G= (CCDC78)	XP_011520660.1:p.Gly505=
XM_011522371.2:c.625G= (CCDC78)	XP_011520673.1:p.Gly209=
XM_017022929.1:c.1513G= (CCDC78)	XP_016878418.1:p.Gly505=
XM_017022930.1:c.613G= (CCDC78)	XP_016878419.1:p.Gly205=
XM_017022931.1:c.-188G= (CCDC78)	XP_016878420.1:n.-188G=
XM_024450150.1:c.343G= (CCDC78)	XP_024305918.1:p.Gly115=
XR_001751835.1:n.1852G= (CCDC78)
XR_001751836.1:n.1831G= (CCDC78)
XR_001751837.1:n.1609G= (CCDC78)
XR_001751838.1:n.1955G= (CCDC78)
XR_001751839.1:n.1417G= (CCDC78)
NM_001031737.3:c.1066G= (CCDC78)	NP_001026907.2:p.Gly356=
NM_001378030.1:c.1066G= (CCDC78) MANE Select	NP_001364959.1:p.Gly356=
NM_001378031.1:c.953+398G= (CCDC78)	NP_001364960.1:n.953+398G=
NM_001378033.1:c.499G= (CCDC78)	NP_001364962.1:p.Gly167=
NR_165382.1:n.1623G= (CCDC78)
NR_165383.1:n.1269G= (CCDC78)
NR_165384.1:n.1234G= (CCDC78)
NR_165385.1:n.1334G= (CCDC78)
NR_165386.1:n.1401G= (CCDC78)