Canonical Allele Identifier: CA778547281
Gene: CCDC178 HGNC NCBI

Linked Data

dbSNP Id: rs1397813667

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.32943370T>G , CM000680.2:g.32943370T>G GRCh38
NC_000018.9:g.30523334T>G , CM000680.1:g.30523334T>G GRCh37
NC_000018.8:g.28777332T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383096.8:c.2524-5279A>C MANE Select ENSP00000372576.3:n.2524-5279A>C
ENST00000300227.12:c.2410-5279A>C ENSP00000300227.8:n.2410-5279A>C
ENST00000383096.7:c.2524-5279A>C ENSP00000372576.3:n.2524-5279A>C
ENST00000403303.5:c.2524-5279A>C ENSP00000385591.1:n.2524-5279A>C
ENST00000406524.6:c.2596-5279A>C ENSP00000385867.2:n.2596-5279A>C
ENST00000579916.5:c.484-5279A>C ENSP00000462153.1:n.484-5279A>C
ENST00000581524.5:c.1015-5279A>C ENSP00000462651.1:n.1015-5279A>C
ENST00000581852.5:c.139-5279A>C ENSP00000464295.1:n.139-5279A>C
ENST00000583930.5:c.2596-5279A>C ENSP00000463254.1:n.2596-5279A>C
NM_001105528.1:c.2524-5279A>C NP_001098998.1:n.2524-5279A>C
NM_001308126.1:c.2596-5279A>C NP_001295055.1:n.2596-5279A>C
NM_198995.2:c.2410-5279A>C NP_945346.2:n.2410-5279A>C
XM_011525948.1:c.2524-5279A>C XP_011524250.1:n.2524-5279A>C
XM_011525951.1:c.2374-5279A>C XP_011524253.1:n.2374-5279A>C
XR_935363.1:n.179+5093T>G
XM_017025721.1:c.2596-5279A>C XP_016881210.1:n.2596-5279A>C
XM_017025722.1:c.2596-5279A>C XP_016881211.1:n.2596-5279A>C
XM_017025723.1:c.2596-5279A>C XP_016881212.1:n.2596-5279A>C
XM_017025724.1:c.2110-5279A>C XP_016881213.1:n.2110-5279A>C
XM_017025725.1:c.2110-5279A>C XP_016881214.1:n.2110-5279A>C
XR_001753402.1:n.179+5093T>G
XR_935363.2:n.179+5093T>G
XR_935365.2:n.179+5093T>G
NM_001105528.3:c.2524-5279A>C NP_001098998.1:n.2524-5279A>C
NM_001308126.3:c.2596-5279A>C NP_001295055.1:n.2596-5279A>C
NM_001371120.1:c.2596-5279A>C NP_001358049.1:n.2596-5279A>C
NM_001371121.1:c.2596-5279A>C NP_001358050.1:n.2596-5279A>C
NM_198995.3:c.2410-5279A>C NP_945346.2:n.2410-5279A>C
NM_001105528.4:c.2524-5279A>C MANE Select NP_001098998.1:n.2524-5279A>C