Canonical Allele Identifier: CA394098471

Gene: CCDC78 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.773918G>T (hg19) ; chr16:g.723918G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.723918G>T , CM000678.2:g.723918G>T	GRCh38
NC_000016.9:g.773918G>T , CM000678.1:g.773918G>T	GRCh37
NC_000016.8:g.713919G>T	NCBI36
NG_032932.1:g.7556C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682391.1:n.1615C>A (CCDC78)
ENST00000345165.10:c.1072C>A (CCDC78) MANE Select	ENSP00000316851.5:p.Leu358Met
ENST00000293889.10:c.1072C>A (CCDC78)	ENSP00000293889.6:p.Leu358Met
ENST00000345165.8:c.618C>A (CCDC78)
ENST00000463539.5:n.1394C>A (CCDC78)
ENST00000466708.5:n.1416C>A (CCDC78)
ENST00000478979.5:n.1719C>A (CCDC78)
ENST00000481804.5:n.2050C>A (CCDC78)
ENST00000482152.1:n.433C>A (CCDC78)
ENST00000482878.5:n.2122C>A (CCDC78)
ENST00000485091.5:n.1225C>A (CCDC78)
ENST00000620831.4:c.-49-38714G>T (MSLN)	ENSP00000482893.1:n.-49-38714G>T
NM_001031737.2:c.1072C>A (CCDC78)	NP_001026907.2:p.Leu358Met
XM_006720838.1:c.1294C>A (CCDC78)	XP_006720901.1:p.Leu432Met
XM_006720843.2:c.1072C>A (CCDC78)	XP_006720906.1:p.Leu358Met
XM_011522356.1:c.1519C>A (CCDC78)	XP_011520658.1:p.Leu507Met
XM_011522357.1:c.1507C>A (CCDC78)	XP_011520659.1:p.Leu503Met
XM_011522358.1:c.1519C>A (CCDC78)	XP_011520660.1:p.Leu507Met
XM_011522359.1:c.1486C>A (CCDC78)	XP_011520661.1:p.Leu496Met
XM_011522360.1:c.1474C>A (CCDC78)	XP_011520662.1:p.Leu492Met
XM_011522361.1:c.1519C>A (CCDC78)	XP_011520663.1:p.Leu507Met
XM_011522362.1:c.1519C>A (CCDC78)	XP_011520664.1:p.Leu507Met
XM_011522363.1:c.1519C>A (CCDC78)	XP_011520665.1:p.Leu507Met
XM_011522364.1:c.1519C>A (CCDC78)	XP_011520666.1:p.Leu507Met
XM_011522365.1:c.1306C>A (CCDC78)	XP_011520667.1:p.Leu436Met
XM_011522366.1:c.1297C>A (CCDC78)	XP_011520668.1:p.Leu433Met
XM_011522367.1:c.1138C>A (CCDC78)	XP_011520669.1:p.Leu380Met
XM_011522368.1:c.1126C>A (CCDC78)	XP_011520670.1:p.Leu376Met
XM_011522369.1:c.1084C>A (CCDC78)	XP_011520671.1:p.Leu362Met
XM_011522370.1:c.916C>A (CCDC78)	XP_011520672.1:p.Leu306Met
XM_011522371.1:c.631C>A (CCDC78)	XP_011520673.1:p.Leu211Met
XM_006720843.4:c.1072C>A (CCDC78)	XP_006720906.1:p.Leu358Met
XM_011522358.2:c.1519C>A (CCDC78)	XP_011520660.1:p.Leu507Met
XM_011522371.2:c.631C>A (CCDC78)	XP_011520673.1:p.Leu211Met
XM_017022929.1:c.1519C>A (CCDC78)	XP_016878418.1:p.Leu507Met
XM_017022930.1:c.619C>A (CCDC78)	XP_016878419.1:p.Leu207Met
XM_017022931.1:c.-182C>A (CCDC78)	XP_016878420.1:n.-182C>A
XM_024450150.1:c.349C>A (CCDC78)	XP_024305918.1:p.Leu117Met
XR_001751835.1:n.1858C>A (CCDC78)
XR_001751836.1:n.1837C>A (CCDC78)
XR_001751837.1:n.1615C>A (CCDC78)
XR_001751838.1:n.1961C>A (CCDC78)
XR_001751839.1:n.1423C>A (CCDC78)
NM_001031737.3:c.1072C>A (CCDC78)	NP_001026907.2:p.Leu358Met
NM_001378030.1:c.1072C>A (CCDC78) MANE Select	NP_001364959.1:p.Leu358Met
NM_001378031.1:c.953+404C>A (CCDC78)	NP_001364960.1:n.953+404C>A
NM_001378033.1:c.505C>A (CCDC78)	NP_001364962.1:p.Leu169Met
NR_165382.1:n.1629C>A (CCDC78)
NR_165383.1:n.1275C>A (CCDC78)
NR_165384.1:n.1240C>A (CCDC78)
NR_165385.1:n.1340C>A (CCDC78)
NR_165386.1:n.1407C>A (CCDC78)