Canonical Allele Identifier: CA394098859

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.774134A>G (hg19) ; chr16:g.724134A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724134A>G , CM000678.2:g.724134A>G	GRCh38
NC_000016.9:g.774134A>G , CM000678.1:g.774134A>G	GRCh37
NC_000016.8:g.714135A>G	NCBI36
NG_032932.1:g.7340T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1568T>C (CCDC78)
ENST00000345165.10:c.1025T>C (CCDC78) MANE Select	ENSP00000316851.5:p.Val342Ala
ENST00000293889.10:c.1025T>C (CCDC78)	ENSP00000293889.6:p.Val342Ala
ENST00000345165.8:c.571T>C (CCDC78)
ENST00000463539.5:n.1347T>C (CCDC78)
ENST00000466708.5:n.1369T>C (CCDC78)
ENST00000478979.5:n.1503T>C (CCDC78)
ENST00000481804.5:n.2003T>C (CCDC78)
ENST00000482152.1:n.386T>C (CCDC78)
ENST00000482878.5:n.1906T>C (CCDC78)
ENST00000485091.5:n.1178T>C (CCDC78)
ENST00000620831.4:c.-49-38498A>G (MSLN)	ENSP00000482893.1:n.-49-38498A>G
NM_001031737.2:c.1025T>C (CCDC78)	NP_001026907.2:p.Val342Ala
XM_006720838.1:c.1247T>C (CCDC78)	XP_006720901.1:p.Val416Ala
XM_006720843.2:c.1025T>C (CCDC78)	XP_006720906.1:p.Val342Ala
XM_011522356.1:c.1472T>C (CCDC78)	XP_011520658.1:p.Val491Ala
XM_011522357.1:c.1460T>C (CCDC78)	XP_011520659.1:p.Val487Ala
XM_011522358.1:c.1472T>C (CCDC78)	XP_011520660.1:p.Val491Ala
XM_011522359.1:c.1439T>C (CCDC78)	XP_011520661.1:p.Val480Ala
XM_011522360.1:c.1427T>C (CCDC78)	XP_011520662.1:p.Val476Ala
XM_011522361.1:c.1472T>C (CCDC78)	XP_011520663.1:p.Val491Ala
XM_011522362.1:c.1472T>C (CCDC78)	XP_011520664.1:p.Val491Ala
XM_011522363.1:c.1472T>C (CCDC78)	XP_011520665.1:p.Val491Ala
XM_011522364.1:c.1472T>C (CCDC78)	XP_011520666.1:p.Val491Ala
XM_011522365.1:c.1259T>C (CCDC78)	XP_011520667.1:p.Val420Ala
XM_011522366.1:c.1250T>C (CCDC78)	XP_011520668.1:p.Val417Ala
XM_011522367.1:c.1091T>C (CCDC78)	XP_011520669.1:p.Val364Ala
XM_011522368.1:c.1079T>C (CCDC78)	XP_011520670.1:p.Val360Ala
XM_011522369.1:c.1037T>C (CCDC78)	XP_011520671.1:p.Val346Ala
XM_011522370.1:c.869T>C (CCDC78)	XP_011520672.1:p.Val290Ala
XM_011522371.1:c.584T>C (CCDC78)	XP_011520673.1:p.Val195Ala
XM_006720843.4:c.1025T>C (CCDC78)	XP_006720906.1:p.Val342Ala
XM_011522358.2:c.1472T>C (CCDC78)	XP_011520660.1:p.Val491Ala
XM_011522371.2:c.584T>C (CCDC78)	XP_011520673.1:p.Val195Ala
XM_017022929.1:c.1472T>C (CCDC78)	XP_016878418.1:p.Val491Ala
XM_017022930.1:c.572T>C (CCDC78)	XP_016878419.1:p.Val191Ala
XM_024450150.1:c.302T>C (CCDC78)	XP_024305918.1:p.Val101Ala
XR_001751835.1:n.1811T>C (CCDC78)
XR_001751836.1:n.1790T>C (CCDC78)
XR_001751837.1:n.1568T>C (CCDC78)
XR_001751838.1:n.1914T>C (CCDC78)
XR_001751839.1:n.1376T>C (CCDC78)
NM_001031737.3:c.1025T>C (CCDC78)	NP_001026907.2:p.Val342Ala
NM_001378030.1:c.1025T>C (CCDC78) MANE Select	NP_001364959.1:p.Val342Ala
NM_001378031.1:c.953+188T>C (CCDC78)	NP_001364960.1:n.953+188T>C
NM_001378033.1:c.458T>C (CCDC78)	NP_001364962.1:p.Val153Ala
NR_165382.1:n.1582T>C (CCDC78)
NR_165383.1:n.1228T>C (CCDC78)
NR_165384.1:n.1193T>C (CCDC78)
NR_165385.1:n.1293T>C (CCDC78)
NR_165386.1:n.1360T>C (CCDC78)