Canonical Allele Identifier: CA2294495232
Gene: CCDC178 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.32943428_32943429delinsTC , CM000680.2:g.32943428_32943429delinsTC GRCh38
NC_000018.9:g.30523392_30523393delinsTC , CM000680.1:g.30523392_30523393delinsTC GRCh37
NC_000018.8:g.28777390_28777391delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383096.8:c.2524-5338_2524-5337delinsGA MANE Select ENSP00000372576.3:n.2524-5338_2524-5337delinsGA
ENST00000300227.12:c.2410-5338_2410-5337delinsGA ENSP00000300227.8:n.2410-5338_2410-5337delinsGA
ENST00000383096.7:c.2524-5338_2524-5337delinsGA ENSP00000372576.3:n.2524-5338_2524-5337delinsGA
ENST00000403303.5:c.2524-5338_2524-5337delinsGA ENSP00000385591.1:n.2524-5338_2524-5337delinsGA
ENST00000406524.6:c.2596-5338_2596-5337delinsGA ENSP00000385867.2:n.2596-5338_2596-5337delinsGA
ENST00000579916.5:c.484-5338_484-5337delinsGA ENSP00000462153.1:n.484-5338_484-5337delinsGA
ENST00000581524.5:c.1015-5338_1015-5337delinsGA ENSP00000462651.1:n.1015-5338_1015-5337delinsGA
ENST00000581852.5:c.139-5338_139-5337delinsGA ENSP00000464295.1:n.139-5338_139-5337delinsGA
ENST00000583930.5:c.2596-5338_2596-5337delinsGA ENSP00000463254.1:n.2596-5338_2596-5337delinsGA
NM_001105528.1:c.2524-5338_2524-5337delinsGA NP_001098998.1:n.2524-5338_2524-5337delinsGA
NM_001308126.1:c.2596-5338_2596-5337delinsGA NP_001295055.1:n.2596-5338_2596-5337delinsGA
NM_198995.2:c.2410-5338_2410-5337delinsGA NP_945346.2:n.2410-5338_2410-5337delinsGA
XM_011525948.1:c.2524-5338_2524-5337delinsGA XP_011524250.1:n.2524-5338_2524-5337delinsGA
XM_011525951.1:c.2374-5338_2374-5337delinsGA XP_011524253.1:n.2374-5338_2374-5337delinsGA
XR_935363.1:n.179+5151_179+5152delinsTC
XM_017025721.1:c.2596-5338_2596-5337delinsGA XP_016881210.1:n.2596-5338_2596-5337delinsGA
XM_017025722.1:c.2596-5338_2596-5337delinsGA XP_016881211.1:n.2596-5338_2596-5337delinsGA
XM_017025723.1:c.2596-5338_2596-5337delinsGA XP_016881212.1:n.2596-5338_2596-5337delinsGA
XM_017025724.1:c.2110-5338_2110-5337delinsGA XP_016881213.1:n.2110-5338_2110-5337delinsGA
XM_017025725.1:c.2110-5338_2110-5337delinsGA XP_016881214.1:n.2110-5338_2110-5337delinsGA
XR_001753402.1:n.179+5151_179+5152delinsTC
XR_935363.2:n.179+5151_179+5152delinsTC
XR_935365.2:n.179+5151_179+5152delinsTC
NM_001105528.3:c.2524-5338_2524-5337delinsGA NP_001098998.1:n.2524-5338_2524-5337delinsGA
NM_001308126.3:c.2596-5338_2596-5337delinsGA NP_001295055.1:n.2596-5338_2596-5337delinsGA
NM_001371120.1:c.2596-5338_2596-5337delinsGA NP_001358049.1:n.2596-5338_2596-5337delinsGA
NM_001371121.1:c.2596-5338_2596-5337delinsGA NP_001358050.1:n.2596-5338_2596-5337delinsGA
NM_198995.3:c.2410-5338_2410-5337delinsGA NP_945346.2:n.2410-5338_2410-5337delinsGA
NM_001105528.4:c.2524-5338_2524-5337delinsGA MANE Select NP_001098998.1:n.2524-5338_2524-5337delinsGA