Canonical Allele Identifier: CA2201211337

Gene: CCDC78 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723886T= , CM000678.2:g.723886T=	GRCh38
NC_000016.9:g.773886T= , CM000678.1:g.773886T=	GRCh37
NC_000016.8:g.713887T=	NCBI36
NG_032932.1:g.7588A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1647A= (CCDC78)
ENST00000345165.10:c.1104A= (CCDC78) MANE Select	ENSP00000316851.5:p.Gly368=
ENST00000293889.10:c.1104A= (CCDC78)	ENSP00000293889.6:p.Gly368=
ENST00000345165.8:c.650A= (CCDC78)
ENST00000463539.5:n.1426A= (CCDC78)
ENST00000466708.5:n.1448A= (CCDC78)
ENST00000478979.5:n.1751A= (CCDC78)
ENST00000481804.5:n.2082A= (CCDC78)
ENST00000482152.1:n.465A= (CCDC78)
ENST00000482878.5:n.2154A= (CCDC78)
ENST00000485091.5:n.1257A= (CCDC78)
ENST00000620831.4:c.-49-38746T= (MSLN)	ENSP00000482893.1:n.-49-38746T=
NM_001031737.2:c.1104A= (CCDC78)	NP_001026907.2:p.Gly368=
XM_006720838.1:c.1326A= (CCDC78)	XP_006720901.1:p.Gly442=
XM_006720843.2:c.1104A= (CCDC78)	XP_006720906.1:p.Gly368=
XM_011522356.1:c.1551A= (CCDC78)	XP_011520658.1:p.Gly517=
XM_011522357.1:c.1539A= (CCDC78)	XP_011520659.1:p.Gly513=
XM_011522358.1:c.1551A= (CCDC78)	XP_011520660.1:p.Gly517=
XM_011522359.1:c.1518A= (CCDC78)	XP_011520661.1:p.Gly506=
XM_011522360.1:c.1506A= (CCDC78)	XP_011520662.1:p.Gly502=
XM_011522361.1:c.1551A= (CCDC78)	XP_011520663.1:p.Gly517=
XM_011522362.1:c.1551A= (CCDC78)	XP_011520664.1:p.Gly517=
XM_011522363.1:c.1551A= (CCDC78)	XP_011520665.1:p.Gly517=
XM_011522364.1:c.1551A= (CCDC78)	XP_011520666.1:p.Gly517=
XM_011522365.1:c.1338A= (CCDC78)	XP_011520667.1:p.Gly446=
XM_011522366.1:c.1329A= (CCDC78)	XP_011520668.1:p.Gly443=
XM_011522367.1:c.1170A= (CCDC78)	XP_011520669.1:p.Gly390=
XM_011522368.1:c.1158A= (CCDC78)	XP_011520670.1:p.Gly386=
XM_011522369.1:c.1116A= (CCDC78)	XP_011520671.1:p.Gly372=
XM_011522370.1:c.948A= (CCDC78)	XP_011520672.1:p.Gly316=
XM_011522371.1:c.663A= (CCDC78)	XP_011520673.1:p.Gly221=
XM_006720843.4:c.1104A= (CCDC78)	XP_006720906.1:p.Gly368=
XM_011522358.2:c.1551A= (CCDC78)	XP_011520660.1:p.Gly517=
XM_011522371.2:c.663A= (CCDC78)	XP_011520673.1:p.Gly221=
XM_017022929.1:c.1551A= (CCDC78)	XP_016878418.1:p.Gly517=
XM_017022930.1:c.651A= (CCDC78)	XP_016878419.1:p.Gly217=
XM_017022931.1:c.-150A= (CCDC78)	XP_016878420.1:n.-150A=
XM_024450150.1:c.381A= (CCDC78)	XP_024305918.1:p.Gly127=
XR_001751835.1:n.1890A= (CCDC78)
XR_001751836.1:n.1869A= (CCDC78)
XR_001751837.1:n.1647A= (CCDC78)
XR_001751838.1:n.1993A= (CCDC78)
XR_001751839.1:n.1455A= (CCDC78)
NM_001031737.3:c.1104A= (CCDC78)	NP_001026907.2:p.Gly368=
NM_001378030.1:c.1104A= (CCDC78) MANE Select	NP_001364959.1:p.Gly368=
NM_001378031.1:c.953+436A= (CCDC78)	NP_001364960.1:n.953+436A=
NM_001378033.1:c.537A= (CCDC78)	NP_001364962.1:p.Gly179=
NR_165382.1:n.1661A= (CCDC78)
NR_165383.1:n.1307A= (CCDC78)
NR_165384.1:n.1272A= (CCDC78)
NR_165385.1:n.1372A= (CCDC78)
NR_165386.1:n.1439A= (CCDC78)