Canonical Allele Identifier: CA394098697

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.774110T>A (hg19) ; chr16:g.724110T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.724110T>A , CM000678.2:g.724110T>A	GRCh38
NC_000016.9:g.774110T>A , CM000678.1:g.774110T>A	GRCh37
NC_000016.8:g.714111T>A	NCBI36
NG_032932.1:g.7364A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1592A>T (CCDC78)
ENST00000345165.10:c.1049A>T (CCDC78) MANE Select	ENSP00000316851.5:p.Asp350Val
ENST00000293889.10:c.1049A>T (CCDC78)	ENSP00000293889.6:p.Asp350Val
ENST00000345165.8:c.595A>T (CCDC78)
ENST00000463539.5:n.1371A>T (CCDC78)
ENST00000466708.5:n.1393A>T (CCDC78)
ENST00000478979.5:n.1527A>T (CCDC78)
ENST00000481804.5:n.2027A>T (CCDC78)
ENST00000482152.1:n.410A>T (CCDC78)
ENST00000482878.5:n.1930A>T (CCDC78)
ENST00000485091.5:n.1202A>T (CCDC78)
ENST00000620831.4:c.-49-38522T>A (MSLN)	ENSP00000482893.1:n.-49-38522T>A
NM_001031737.2:c.1049A>T (CCDC78)	NP_001026907.2:p.Asp350Val
XM_006720838.1:c.1271A>T (CCDC78)	XP_006720901.1:p.Asp424Val
XM_006720843.2:c.1049A>T (CCDC78)	XP_006720906.1:p.Asp350Val
XM_011522356.1:c.1496A>T (CCDC78)	XP_011520658.1:p.Asp499Val
XM_011522357.1:c.1484A>T (CCDC78)	XP_011520659.1:p.Asp495Val
XM_011522358.1:c.1496A>T (CCDC78)	XP_011520660.1:p.Asp499Val
XM_011522359.1:c.1463A>T (CCDC78)	XP_011520661.1:p.Asp488Val
XM_011522360.1:c.1451A>T (CCDC78)	XP_011520662.1:p.Asp484Val
XM_011522361.1:c.1496A>T (CCDC78)	XP_011520663.1:p.Asp499Val
XM_011522362.1:c.1496A>T (CCDC78)	XP_011520664.1:p.Asp499Val
XM_011522363.1:c.1496A>T (CCDC78)	XP_011520665.1:p.Asp499Val
XM_011522364.1:c.1496A>T (CCDC78)	XP_011520666.1:p.Asp499Val
XM_011522365.1:c.1283A>T (CCDC78)	XP_011520667.1:p.Asp428Val
XM_011522366.1:c.1274A>T (CCDC78)	XP_011520668.1:p.Asp425Val
XM_011522367.1:c.1115A>T (CCDC78)	XP_011520669.1:p.Asp372Val
XM_011522368.1:c.1103A>T (CCDC78)	XP_011520670.1:p.Asp368Val
XM_011522369.1:c.1061A>T (CCDC78)	XP_011520671.1:p.Asp354Val
XM_011522370.1:c.893A>T (CCDC78)	XP_011520672.1:p.Asp298Val
XM_011522371.1:c.608A>T (CCDC78)	XP_011520673.1:p.Asp203Val
XM_006720843.4:c.1049A>T (CCDC78)	XP_006720906.1:p.Asp350Val
XM_011522358.2:c.1496A>T (CCDC78)	XP_011520660.1:p.Asp499Val
XM_011522371.2:c.608A>T (CCDC78)	XP_011520673.1:p.Asp203Val
XM_017022929.1:c.1496A>T (CCDC78)	XP_016878418.1:p.Asp499Val
XM_017022930.1:c.596A>T (CCDC78)	XP_016878419.1:p.Asp199Val
XM_024450150.1:c.326A>T (CCDC78)	XP_024305918.1:p.Asp109Val
XR_001751835.1:n.1835A>T (CCDC78)
XR_001751836.1:n.1814A>T (CCDC78)
XR_001751837.1:n.1592A>T (CCDC78)
XR_001751838.1:n.1938A>T (CCDC78)
XR_001751839.1:n.1400A>T (CCDC78)
NM_001031737.3:c.1049A>T (CCDC78)	NP_001026907.2:p.Asp350Val
NM_001378030.1:c.1049A>T (CCDC78) MANE Select	NP_001364959.1:p.Asp350Val
NM_001378031.1:c.953+212A>T (CCDC78)	NP_001364960.1:n.953+212A>T
NM_001378033.1:c.482A>T (CCDC78)	NP_001364962.1:p.Asp161Val
NR_165382.1:n.1606A>T (CCDC78)
NR_165383.1:n.1252A>T (CCDC78)
NR_165384.1:n.1217A>T (CCDC78)
NR_165385.1:n.1317A>T (CCDC78)
NR_165386.1:n.1384A>T (CCDC78)