Canonical Allele Identifier: CA2201211491

Gene: CCDC78 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724124G= , CM000678.2:g.724124G=	GRCh38
NC_000016.9:g.774124G= , CM000678.1:g.774124G=	GRCh37
NC_000016.8:g.714125G=	NCBI36
NG_032932.1:g.7350C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1578C= (CCDC78)
ENST00000345165.10:c.1035C= (CCDC78) MANE Select	ENSP00000316851.5:p.Phe345=
ENST00000293889.10:c.1035C= (CCDC78)	ENSP00000293889.6:p.Phe345=
ENST00000345165.8:c.581C= (CCDC78)
ENST00000463539.5:n.1357C= (CCDC78)
ENST00000466708.5:n.1379C= (CCDC78)
ENST00000478979.5:n.1513C= (CCDC78)
ENST00000481804.5:n.2013C= (CCDC78)
ENST00000482152.1:n.396C= (CCDC78)
ENST00000482878.5:n.1916C= (CCDC78)
ENST00000485091.5:n.1188C= (CCDC78)
ENST00000620831.4:c.-49-38508G= (MSLN)	ENSP00000482893.1:n.-49-38508G=
NM_001031737.2:c.1035C= (CCDC78)	NP_001026907.2:p.Phe345=
XM_006720838.1:c.1257C= (CCDC78)	XP_006720901.1:p.Phe419=
XM_006720843.2:c.1035C= (CCDC78)	XP_006720906.1:p.Phe345=
XM_011522356.1:c.1482C= (CCDC78)	XP_011520658.1:p.Phe494=
XM_011522357.1:c.1470C= (CCDC78)	XP_011520659.1:p.Phe490=
XM_011522358.1:c.1482C= (CCDC78)	XP_011520660.1:p.Phe494=
XM_011522359.1:c.1449C= (CCDC78)	XP_011520661.1:p.Phe483=
XM_011522360.1:c.1437C= (CCDC78)	XP_011520662.1:p.Phe479=
XM_011522361.1:c.1482C= (CCDC78)	XP_011520663.1:p.Phe494=
XM_011522362.1:c.1482C= (CCDC78)	XP_011520664.1:p.Phe494=
XM_011522363.1:c.1482C= (CCDC78)	XP_011520665.1:p.Phe494=
XM_011522364.1:c.1482C= (CCDC78)	XP_011520666.1:p.Phe494=
XM_011522365.1:c.1269C= (CCDC78)	XP_011520667.1:p.Phe423=
XM_011522366.1:c.1260C= (CCDC78)	XP_011520668.1:p.Phe420=
XM_011522367.1:c.1101C= (CCDC78)	XP_011520669.1:p.Phe367=
XM_011522368.1:c.1089C= (CCDC78)	XP_011520670.1:p.Phe363=
XM_011522369.1:c.1047C= (CCDC78)	XP_011520671.1:p.Phe349=
XM_011522370.1:c.879C= (CCDC78)	XP_011520672.1:p.Phe293=
XM_011522371.1:c.594C= (CCDC78)	XP_011520673.1:p.Phe198=
XM_006720843.4:c.1035C= (CCDC78)	XP_006720906.1:p.Phe345=
XM_011522358.2:c.1482C= (CCDC78)	XP_011520660.1:p.Phe494=
XM_011522371.2:c.594C= (CCDC78)	XP_011520673.1:p.Phe198=
XM_017022929.1:c.1482C= (CCDC78)	XP_016878418.1:p.Phe494=
XM_017022930.1:c.582C= (CCDC78)	XP_016878419.1:p.Phe194=
XM_024450150.1:c.312C= (CCDC78)	XP_024305918.1:p.Phe104=
XR_001751835.1:n.1821C= (CCDC78)
XR_001751836.1:n.1800C= (CCDC78)
XR_001751837.1:n.1578C= (CCDC78)
XR_001751838.1:n.1924C= (CCDC78)
XR_001751839.1:n.1386C= (CCDC78)
NM_001031737.3:c.1035C= (CCDC78)	NP_001026907.2:p.Phe345=
NM_001378030.1:c.1035C= (CCDC78) MANE Select	NP_001364959.1:p.Phe345=
NM_001378031.1:c.953+198C= (CCDC78)	NP_001364960.1:n.953+198C=
NM_001378033.1:c.468C= (CCDC78)	NP_001364962.1:p.Phe156=
NR_165382.1:n.1592C= (CCDC78)
NR_165383.1:n.1238C= (CCDC78)
NR_165384.1:n.1203C= (CCDC78)
NR_165385.1:n.1303C= (CCDC78)
NR_165386.1:n.1370C= (CCDC78)