Canonical Allele Identifier: CA394098536

Gene: CCDC78 MSLN

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1601G>C (CCDC78)
ENST00000345165.10:c.1058G>C (CCDC78) MANE Select	ENSP00000316851.5:p.Gly353Ala
ENST00000293889.10:c.1058G>C (CCDC78)	ENSP00000293889.6:p.Gly353Ala
ENST00000345165.8:c.604G>C (CCDC78)
ENST00000463539.5:n.1380G>C (CCDC78)
ENST00000466708.5:n.1402G>C (CCDC78)
ENST00000478979.5:n.1705G>C (CCDC78)
ENST00000481804.5:n.2036G>C (CCDC78)
ENST00000482152.1:n.419G>C (CCDC78)
ENST00000482878.5:n.2108G>C (CCDC78)
ENST00000485091.5:n.1211G>C (CCDC78)
ENST00000620831.4:c.-49-38700C>G (MSLN)	ENSP00000482893.1:n.-49-38700C>G
NM_001031737.2:c.1058G>C (CCDC78)	NP_001026907.2:p.Gly353Ala
XM_006720838.1:c.1280G>C (CCDC78)	XP_006720901.1:p.Gly427Ala
XM_006720843.2:c.1058G>C (CCDC78)	XP_006720906.1:p.Gly353Ala
XM_011522356.1:c.1505G>C (CCDC78)	XP_011520658.1:p.Gly502Ala
XM_011522357.1:c.1493G>C (CCDC78)	XP_011520659.1:p.Gly498Ala
XM_011522358.1:c.1505G>C (CCDC78)	XP_011520660.1:p.Gly502Ala
XM_011522359.1:c.1472G>C (CCDC78)	XP_011520661.1:p.Gly491Ala
XM_011522360.1:c.1460G>C (CCDC78)	XP_011520662.1:p.Gly487Ala
XM_011522361.1:c.1505G>C (CCDC78)	XP_011520663.1:p.Gly502Ala
XM_011522362.1:c.1505G>C (CCDC78)	XP_011520664.1:p.Gly502Ala
XM_011522363.1:c.1505G>C (CCDC78)	XP_011520665.1:p.Gly502Ala
XM_011522364.1:c.1505G>C (CCDC78)	XP_011520666.1:p.Gly502Ala
XM_011522365.1:c.1292G>C (CCDC78)	XP_011520667.1:p.Gly431Ala
XM_011522366.1:c.1283G>C (CCDC78)	XP_011520668.1:p.Gly428Ala
XM_011522367.1:c.1124G>C (CCDC78)	XP_011520669.1:p.Gly375Ala
XM_011522368.1:c.1112G>C (CCDC78)	XP_011520670.1:p.Gly371Ala
XM_011522369.1:c.1070G>C (CCDC78)	XP_011520671.1:p.Gly357Ala
XM_011522370.1:c.902G>C (CCDC78)	XP_011520672.1:p.Gly301Ala
XM_011522371.1:c.617G>C (CCDC78)	XP_011520673.1:p.Gly206Ala
XM_006720843.4:c.1058G>C (CCDC78)	XP_006720906.1:p.Gly353Ala
XM_011522358.2:c.1505G>C (CCDC78)	XP_011520660.1:p.Gly502Ala
XM_011522371.2:c.617G>C (CCDC78)	XP_011520673.1:p.Gly206Ala
XM_017022929.1:c.1505G>C (CCDC78)	XP_016878418.1:p.Gly502Ala
XM_017022930.1:c.605G>C (CCDC78)	XP_016878419.1:p.Gly202Ala
XM_017022931.1:c.-196G>C (CCDC78)	XP_016878420.1:n.-196G>C
XM_024450150.1:c.335G>C (CCDC78)	XP_024305918.1:p.Gly112Ala
XR_001751835.1:n.1844G>C (CCDC78)
XR_001751836.1:n.1823G>C (CCDC78)
XR_001751837.1:n.1601G>C (CCDC78)
XR_001751838.1:n.1947G>C (CCDC78)
XR_001751839.1:n.1409G>C (CCDC78)
NM_001031737.3:c.1058G>C (CCDC78)	NP_001026907.2:p.Gly353Ala
NM_001378030.1:c.1058G>C (CCDC78) MANE Select	NP_001364959.1:p.Gly353Ala
NM_001378031.1:c.953+390G>C (CCDC78)	NP_001364960.1:n.953+390G>C
NM_001378033.1:c.491G>C (CCDC78)	NP_001364962.1:p.Gly164Ala
NR_165382.1:n.1615G>C (CCDC78)
NR_165383.1:n.1261G>C (CCDC78)
NR_165384.1:n.1226G>C (CCDC78)
NR_165385.1:n.1326G>C (CCDC78)
NR_165386.1:n.1393G>C (CCDC78)