Canonical Allele Identifier: CA394098884

Gene: CCDC78 MSLN

Linked Data

• gnomAD v4: 16-724141-G-T
• MyVariant Identifiers: chr16:g.774141G>T (hg19) ; chr16:g.724141G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724141G>T , CM000678.2:g.724141G>T	GRCh38
NC_000016.9:g.774141G>T , CM000678.1:g.774141G>T	GRCh37
NC_000016.8:g.714142G>T	NCBI36
NG_032932.1:g.7333C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1561C>A (CCDC78)
ENST00000345165.10:c.1018C>A (CCDC78) MANE Select	ENSP00000316851.5:p.Pro340Thr
ENST00000293889.10:c.1018C>A (CCDC78)	ENSP00000293889.6:p.Pro340Thr
ENST00000345165.8:c.564C>A (CCDC78)
ENST00000463539.5:n.1340C>A (CCDC78)
ENST00000466708.5:n.1362C>A (CCDC78)
ENST00000478979.5:n.1496C>A (CCDC78)
ENST00000481804.5:n.1996C>A (CCDC78)
ENST00000482152.1:n.379C>A (CCDC78)
ENST00000482878.5:n.1899C>A (CCDC78)
ENST00000485091.5:n.1171C>A (CCDC78)
ENST00000620831.4:c.-49-38491G>T (MSLN)	ENSP00000482893.1:n.-49-38491G>T
NM_001031737.2:c.1018C>A (CCDC78)	NP_001026907.2:p.Pro340Thr
XM_006720838.1:c.1240C>A (CCDC78)	XP_006720901.1:p.Pro414Thr
XM_006720843.2:c.1018C>A (CCDC78)	XP_006720906.1:p.Pro340Thr
XM_011522356.1:c.1465C>A (CCDC78)	XP_011520658.1:p.Pro489Thr
XM_011522357.1:c.1453C>A (CCDC78)	XP_011520659.1:p.Pro485Thr
XM_011522358.1:c.1465C>A (CCDC78)	XP_011520660.1:p.Pro489Thr
XM_011522359.1:c.1432C>A (CCDC78)	XP_011520661.1:p.Pro478Thr
XM_011522360.1:c.1420C>A (CCDC78)	XP_011520662.1:p.Pro474Thr
XM_011522361.1:c.1465C>A (CCDC78)	XP_011520663.1:p.Pro489Thr
XM_011522362.1:c.1465C>A (CCDC78)	XP_011520664.1:p.Pro489Thr
XM_011522363.1:c.1465C>A (CCDC78)	XP_011520665.1:p.Pro489Thr
XM_011522364.1:c.1465C>A (CCDC78)	XP_011520666.1:p.Pro489Thr
XM_011522365.1:c.1252C>A (CCDC78)	XP_011520667.1:p.Pro418Thr
XM_011522366.1:c.1243C>A (CCDC78)	XP_011520668.1:p.Pro415Thr
XM_011522367.1:c.1084C>A (CCDC78)	XP_011520669.1:p.Pro362Thr
XM_011522368.1:c.1072C>A (CCDC78)	XP_011520670.1:p.Pro358Thr
XM_011522369.1:c.1030C>A (CCDC78)	XP_011520671.1:p.Pro344Thr
XM_011522370.1:c.862C>A (CCDC78)	XP_011520672.1:p.Pro288Thr
XM_011522371.1:c.577C>A (CCDC78)	XP_011520673.1:p.Pro193Thr
XM_006720843.4:c.1018C>A (CCDC78)	XP_006720906.1:p.Pro340Thr
XM_011522358.2:c.1465C>A (CCDC78)	XP_011520660.1:p.Pro489Thr
XM_011522371.2:c.577C>A (CCDC78)	XP_011520673.1:p.Pro193Thr
XM_017022929.1:c.1465C>A (CCDC78)	XP_016878418.1:p.Pro489Thr
XM_017022930.1:c.565C>A (CCDC78)	XP_016878419.1:p.Pro189Thr
XM_024450150.1:c.295C>A (CCDC78)	XP_024305918.1:p.Pro99Thr
XR_001751835.1:n.1804C>A (CCDC78)
XR_001751836.1:n.1783C>A (CCDC78)
XR_001751837.1:n.1561C>A (CCDC78)
XR_001751838.1:n.1907C>A (CCDC78)
XR_001751839.1:n.1369C>A (CCDC78)
NM_001031737.3:c.1018C>A (CCDC78)	NP_001026907.2:p.Pro340Thr
NM_001378030.1:c.1018C>A (CCDC78) MANE Select	NP_001364959.1:p.Pro340Thr
NM_001378031.1:c.953+181C>A (CCDC78)	NP_001364960.1:n.953+181C>A
NM_001378033.1:c.451C>A (CCDC78)	NP_001364962.1:p.Pro151Thr
NR_165382.1:n.1575C>A (CCDC78)
NR_165383.1:n.1221C>A (CCDC78)
NR_165384.1:n.1186C>A (CCDC78)
NR_165385.1:n.1286C>A (CCDC78)
NR_165386.1:n.1353C>A (CCDC78)