Canonical Allele Identifier: CA394098530

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.773932C>T (hg19) ; chr16:g.723932C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723932C>T , CM000678.2:g.723932C>T	GRCh38
NC_000016.9:g.773932C>T , CM000678.1:g.773932C>T	GRCh37
NC_000016.8:g.713933C>T	NCBI36
NG_032932.1:g.7542G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1601G>A (CCDC78)
ENST00000345165.10:c.1058G>A (CCDC78) MANE Select	ENSP00000316851.5:p.Gly353Asp
ENST00000293889.10:c.1058G>A (CCDC78)	ENSP00000293889.6:p.Gly353Asp
ENST00000345165.8:c.604G>A (CCDC78)
ENST00000463539.5:n.1380G>A (CCDC78)
ENST00000466708.5:n.1402G>A (CCDC78)
ENST00000478979.5:n.1705G>A (CCDC78)
ENST00000481804.5:n.2036G>A (CCDC78)
ENST00000482152.1:n.419G>A (CCDC78)
ENST00000482878.5:n.2108G>A (CCDC78)
ENST00000485091.5:n.1211G>A (CCDC78)
ENST00000620831.4:c.-49-38700C>T (MSLN)	ENSP00000482893.1:n.-49-38700C>T
NM_001031737.2:c.1058G>A (CCDC78)	NP_001026907.2:p.Gly353Asp
XM_006720838.1:c.1280G>A (CCDC78)	XP_006720901.1:p.Gly427Asp
XM_006720843.2:c.1058G>A (CCDC78)	XP_006720906.1:p.Gly353Asp
XM_011522356.1:c.1505G>A (CCDC78)	XP_011520658.1:p.Gly502Asp
XM_011522357.1:c.1493G>A (CCDC78)	XP_011520659.1:p.Gly498Asp
XM_011522358.1:c.1505G>A (CCDC78)	XP_011520660.1:p.Gly502Asp
XM_011522359.1:c.1472G>A (CCDC78)	XP_011520661.1:p.Gly491Asp
XM_011522360.1:c.1460G>A (CCDC78)	XP_011520662.1:p.Gly487Asp
XM_011522361.1:c.1505G>A (CCDC78)	XP_011520663.1:p.Gly502Asp
XM_011522362.1:c.1505G>A (CCDC78)	XP_011520664.1:p.Gly502Asp
XM_011522363.1:c.1505G>A (CCDC78)	XP_011520665.1:p.Gly502Asp
XM_011522364.1:c.1505G>A (CCDC78)	XP_011520666.1:p.Gly502Asp
XM_011522365.1:c.1292G>A (CCDC78)	XP_011520667.1:p.Gly431Asp
XM_011522366.1:c.1283G>A (CCDC78)	XP_011520668.1:p.Gly428Asp
XM_011522367.1:c.1124G>A (CCDC78)	XP_011520669.1:p.Gly375Asp
XM_011522368.1:c.1112G>A (CCDC78)	XP_011520670.1:p.Gly371Asp
XM_011522369.1:c.1070G>A (CCDC78)	XP_011520671.1:p.Gly357Asp
XM_011522370.1:c.902G>A (CCDC78)	XP_011520672.1:p.Gly301Asp
XM_011522371.1:c.617G>A (CCDC78)	XP_011520673.1:p.Gly206Asp
XM_006720843.4:c.1058G>A (CCDC78)	XP_006720906.1:p.Gly353Asp
XM_011522358.2:c.1505G>A (CCDC78)	XP_011520660.1:p.Gly502Asp
XM_011522371.2:c.617G>A (CCDC78)	XP_011520673.1:p.Gly206Asp
XM_017022929.1:c.1505G>A (CCDC78)	XP_016878418.1:p.Gly502Asp
XM_017022930.1:c.605G>A (CCDC78)	XP_016878419.1:p.Gly202Asp
XM_017022931.1:c.-196G>A (CCDC78)	XP_016878420.1:n.-196G>A
XM_024450150.1:c.335G>A (CCDC78)	XP_024305918.1:p.Gly112Asp
XR_001751835.1:n.1844G>A (CCDC78)
XR_001751836.1:n.1823G>A (CCDC78)
XR_001751837.1:n.1601G>A (CCDC78)
XR_001751838.1:n.1947G>A (CCDC78)
XR_001751839.1:n.1409G>A (CCDC78)
NM_001031737.3:c.1058G>A (CCDC78)	NP_001026907.2:p.Gly353Asp
NM_001378030.1:c.1058G>A (CCDC78) MANE Select	NP_001364959.1:p.Gly353Asp
NM_001378031.1:c.953+390G>A (CCDC78)	NP_001364960.1:n.953+390G>A
NM_001378033.1:c.491G>A (CCDC78)	NP_001364962.1:p.Gly164Asp
NR_165382.1:n.1615G>A (CCDC78)
NR_165383.1:n.1261G>A (CCDC78)
NR_165384.1:n.1226G>A (CCDC78)
NR_165385.1:n.1326G>A (CCDC78)
NR_165386.1:n.1393G>A (CCDC78)