Canonical Allele Identifier: CA394098420

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.773902T>G (hg19) ; chr16:g.723902T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723902T>G , CM000678.2:g.723902T>G	GRCh38
NC_000016.9:g.773902T>G , CM000678.1:g.773902T>G	GRCh37
NC_000016.8:g.713903T>G	NCBI36
NG_032932.1:g.7572A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1631A>C (CCDC78)
ENST00000345165.10:c.1088A>C (CCDC78) MANE Select	ENSP00000316851.5:p.Lys363Thr
ENST00000293889.10:c.1088A>C (CCDC78)	ENSP00000293889.6:p.Lys363Thr
ENST00000345165.8:c.634A>C (CCDC78)
ENST00000463539.5:n.1410A>C (CCDC78)
ENST00000466708.5:n.1432A>C (CCDC78)
ENST00000478979.5:n.1735A>C (CCDC78)
ENST00000481804.5:n.2066A>C (CCDC78)
ENST00000482152.1:n.449A>C (CCDC78)
ENST00000482878.5:n.2138A>C (CCDC78)
ENST00000485091.5:n.1241A>C (CCDC78)
ENST00000620831.4:c.-49-38730T>G (MSLN)	ENSP00000482893.1:n.-49-38730T>G
NM_001031737.2:c.1088A>C (CCDC78)	NP_001026907.2:p.Lys363Thr
XM_006720838.1:c.1310A>C (CCDC78)	XP_006720901.1:p.Lys437Thr
XM_006720843.2:c.1088A>C (CCDC78)	XP_006720906.1:p.Lys363Thr
XM_011522356.1:c.1535A>C (CCDC78)	XP_011520658.1:p.Lys512Thr
XM_011522357.1:c.1523A>C (CCDC78)	XP_011520659.1:p.Lys508Thr
XM_011522358.1:c.1535A>C (CCDC78)	XP_011520660.1:p.Lys512Thr
XM_011522359.1:c.1502A>C (CCDC78)	XP_011520661.1:p.Lys501Thr
XM_011522360.1:c.1490A>C (CCDC78)	XP_011520662.1:p.Lys497Thr
XM_011522361.1:c.1535A>C (CCDC78)	XP_011520663.1:p.Lys512Thr
XM_011522362.1:c.1535A>C (CCDC78)	XP_011520664.1:p.Lys512Thr
XM_011522363.1:c.1535A>C (CCDC78)	XP_011520665.1:p.Lys512Thr
XM_011522364.1:c.1535A>C (CCDC78)	XP_011520666.1:p.Lys512Thr
XM_011522365.1:c.1322A>C (CCDC78)	XP_011520667.1:p.Lys441Thr
XM_011522366.1:c.1313A>C (CCDC78)	XP_011520668.1:p.Lys438Thr
XM_011522367.1:c.1154A>C (CCDC78)	XP_011520669.1:p.Lys385Thr
XM_011522368.1:c.1142A>C (CCDC78)	XP_011520670.1:p.Lys381Thr
XM_011522369.1:c.1100A>C (CCDC78)	XP_011520671.1:p.Lys367Thr
XM_011522370.1:c.932A>C (CCDC78)	XP_011520672.1:p.Lys311Thr
XM_011522371.1:c.647A>C (CCDC78)	XP_011520673.1:p.Lys216Thr
XM_006720843.4:c.1088A>C (CCDC78)	XP_006720906.1:p.Lys363Thr
XM_011522358.2:c.1535A>C (CCDC78)	XP_011520660.1:p.Lys512Thr
XM_011522371.2:c.647A>C (CCDC78)	XP_011520673.1:p.Lys216Thr
XM_017022929.1:c.1535A>C (CCDC78)	XP_016878418.1:p.Lys512Thr
XM_017022930.1:c.635A>C (CCDC78)	XP_016878419.1:p.Lys212Thr
XM_017022931.1:c.-166A>C (CCDC78)	XP_016878420.1:n.-166A>C
XM_024450150.1:c.365A>C (CCDC78)	XP_024305918.1:p.Lys122Thr
XR_001751835.1:n.1874A>C (CCDC78)
XR_001751836.1:n.1853A>C (CCDC78)
XR_001751837.1:n.1631A>C (CCDC78)
XR_001751838.1:n.1977A>C (CCDC78)
XR_001751839.1:n.1439A>C (CCDC78)
NM_001031737.3:c.1088A>C (CCDC78)	NP_001026907.2:p.Lys363Thr
NM_001378030.1:c.1088A>C (CCDC78) MANE Select	NP_001364959.1:p.Lys363Thr
NM_001378031.1:c.953+420A>C (CCDC78)	NP_001364960.1:n.953+420A>C
NM_001378033.1:c.521A>C (CCDC78)	NP_001364962.1:p.Lys174Thr
NR_165382.1:n.1645A>C (CCDC78)
NR_165383.1:n.1291A>C (CCDC78)
NR_165384.1:n.1256A>C (CCDC78)
NR_165385.1:n.1356A>C (CCDC78)
NR_165386.1:n.1423A>C (CCDC78)