Canonical Allele Identifier: CA394099158

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.774193G>C (hg19) ; chr16:g.724193G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724193G>C , CM000678.2:g.724193G>C	GRCh38
NC_000016.9:g.774193G>C , CM000678.1:g.774193G>C	GRCh37
NC_000016.8:g.714194G>C	NCBI36
NG_032932.1:g.7281C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1509C>G (CCDC78)
ENST00000345165.10:c.966C>G (CCDC78) MANE Select	ENSP00000316851.5:p.Asn322Lys
ENST00000293889.10:c.966C>G (CCDC78)	ENSP00000293889.6:p.Asn322Lys
ENST00000345165.8:c.512C>G (CCDC78)
ENST00000463539.5:n.1288C>G (CCDC78)
ENST00000466708.5:n.1310C>G (CCDC78)
ENST00000478979.5:n.1444C>G (CCDC78)
ENST00000481804.5:n.1944C>G (CCDC78)
ENST00000482152.1:n.327C>G (CCDC78)
ENST00000482878.5:n.1847C>G (CCDC78)
ENST00000485091.5:n.1119C>G (CCDC78)
ENST00000620831.4:c.-49-38439G>C (MSLN)	ENSP00000482893.1:n.-49-38439G>C
NM_001031737.2:c.966C>G (CCDC78)	NP_001026907.2:p.Asn322Lys
XM_006720838.1:c.1188C>G (CCDC78)	XP_006720901.1:p.Asn396Lys
XM_006720843.2:c.966C>G (CCDC78)	XP_006720906.1:p.Asn322Lys
XM_011522356.1:c.1413C>G (CCDC78)	XP_011520658.1:p.Asn471Lys
XM_011522357.1:c.1401C>G (CCDC78)	XP_011520659.1:p.Asn467Lys
XM_011522358.1:c.1413C>G (CCDC78)	XP_011520660.1:p.Asn471Lys
XM_011522359.1:c.1380C>G (CCDC78)	XP_011520661.1:p.Asn460Lys
XM_011522360.1:c.1368C>G (CCDC78)	XP_011520662.1:p.Asn456Lys
XM_011522361.1:c.1413C>G (CCDC78)	XP_011520663.1:p.Asn471Lys
XM_011522362.1:c.1413C>G (CCDC78)	XP_011520664.1:p.Asn471Lys
XM_011522363.1:c.1413C>G (CCDC78)	XP_011520665.1:p.Asn471Lys
XM_011522364.1:c.1413C>G (CCDC78)	XP_011520666.1:p.Asn471Lys
XM_011522365.1:c.1200C>G (CCDC78)	XP_011520667.1:p.Asn400Lys
XM_011522366.1:c.1191C>G (CCDC78)	XP_011520668.1:p.Asn397Lys
XM_011522367.1:c.1032C>G (CCDC78)	XP_011520669.1:p.Asn344Lys
XM_011522368.1:c.1020C>G (CCDC78)	XP_011520670.1:p.Asn340Lys
XM_011522369.1:c.978C>G (CCDC78)	XP_011520671.1:p.Asn326Lys
XM_011522370.1:c.810C>G (CCDC78)	XP_011520672.1:p.Asn270Lys
XM_011522371.1:c.525C>G (CCDC78)	XP_011520673.1:p.Asn175Lys
XM_006720843.4:c.966C>G (CCDC78)	XP_006720906.1:p.Asn322Lys
XM_011522358.2:c.1413C>G (CCDC78)	XP_011520660.1:p.Asn471Lys
XM_011522371.2:c.525C>G (CCDC78)	XP_011520673.1:p.Asn175Lys
XM_017022929.1:c.1413C>G (CCDC78)	XP_016878418.1:p.Asn471Lys
XM_017022930.1:c.513C>G (CCDC78)	XP_016878419.1:p.Asn171Lys
XM_024450150.1:c.243C>G (CCDC78)	XP_024305918.1:p.Asn81Lys
XR_001751835.1:n.1752C>G (CCDC78)
XR_001751836.1:n.1731C>G (CCDC78)
XR_001751837.1:n.1509C>G (CCDC78)
XR_001751838.1:n.1855C>G (CCDC78)
XR_001751839.1:n.1317C>G (CCDC78)
NM_001031737.3:c.966C>G (CCDC78)	NP_001026907.2:p.Asn322Lys
NM_001378030.1:c.966C>G (CCDC78) MANE Select	NP_001364959.1:p.Asn322Lys
NM_001378031.1:c.953+129C>G (CCDC78)	NP_001364960.1:n.953+129C>G
NM_001378033.1:c.399C>G (CCDC78)	NP_001364962.1:p.Asn133Lys
NR_165382.1:n.1523C>G (CCDC78)
NR_165383.1:n.1169C>G (CCDC78)
NR_165384.1:n.1134C>G (CCDC78)
NR_165385.1:n.1234C>G (CCDC78)
NR_165386.1:n.1301C>G (CCDC78)