Canonical Allele Identifier: CA778547318

Gene: CCDC178

Linked Data

• dbSNP Id: rs1246299887
• MyVariant Identifiers: chr18:g.30523414_30523415insC (hg19) ; chr18:g.32943450_32943451insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.32943450_32943451insC , CM000680.2:g.32943450_32943451insC	GRCh38
NC_000018.9:g.30523414_30523415insC , CM000680.1:g.30523414_30523415insC	GRCh37
NC_000018.8:g.28777412_28777413insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383096.8:c.2524-5360_2524-5359insG MANE Select	ENSP00000372576.3:n.2524-5360_2524-5359insG
ENST00000300227.12:c.2410-5360_2410-5359insG	ENSP00000300227.8:n.2410-5360_2410-5359insG
ENST00000383096.7:c.2524-5360_2524-5359insG	ENSP00000372576.3:n.2524-5360_2524-5359insG
ENST00000403303.5:c.2524-5360_2524-5359insG	ENSP00000385591.1:n.2524-5360_2524-5359insG
ENST00000406524.6:c.2596-5360_2596-5359insG	ENSP00000385867.2:n.2596-5360_2596-5359insG
ENST00000579916.5:c.484-5360_484-5359insG	ENSP00000462153.1:n.484-5360_484-5359insG
ENST00000581524.5:c.1015-5360_1015-5359insG	ENSP00000462651.1:n.1015-5360_1015-5359insG
ENST00000581852.5:c.139-5360_139-5359insG	ENSP00000464295.1:n.139-5360_139-5359insG
ENST00000583930.5:c.2596-5360_2596-5359insG	ENSP00000463254.1:n.2596-5360_2596-5359insG
NM_001105528.1:c.2524-5360_2524-5359insG	NP_001098998.1:n.2524-5360_2524-5359insG
NM_001308126.1:c.2596-5360_2596-5359insG	NP_001295055.1:n.2596-5360_2596-5359insG
NM_198995.2:c.2410-5360_2410-5359insG	NP_945346.2:n.2410-5360_2410-5359insG
XM_011525948.1:c.2524-5360_2524-5359insG	XP_011524250.1:n.2524-5360_2524-5359insG
XM_011525951.1:c.2374-5360_2374-5359insG	XP_011524253.1:n.2374-5360_2374-5359insG
XR_935363.1:n.179+5173_179+5174insC
XM_017025721.1:c.2596-5360_2596-5359insG	XP_016881210.1:n.2596-5360_2596-5359insG
XM_017025722.1:c.2596-5360_2596-5359insG	XP_016881211.1:n.2596-5360_2596-5359insG
XM_017025723.1:c.2596-5360_2596-5359insG	XP_016881212.1:n.2596-5360_2596-5359insG
XM_017025724.1:c.2110-5360_2110-5359insG	XP_016881213.1:n.2110-5360_2110-5359insG
XM_017025725.1:c.2110-5360_2110-5359insG	XP_016881214.1:n.2110-5360_2110-5359insG
XR_001753402.1:n.179+5173_179+5174insC
XR_935363.2:n.179+5173_179+5174insC
XR_935365.2:n.179+5173_179+5174insC
NM_001105528.3:c.2524-5360_2524-5359insG	NP_001098998.1:n.2524-5360_2524-5359insG
NM_001308126.3:c.2596-5360_2596-5359insG	NP_001295055.1:n.2596-5360_2596-5359insG
NM_001371120.1:c.2596-5360_2596-5359insG	NP_001358049.1:n.2596-5360_2596-5359insG
NM_001371121.1:c.2596-5360_2596-5359insG	NP_001358050.1:n.2596-5360_2596-5359insG
NM_198995.3:c.2410-5360_2410-5359insG	NP_945346.2:n.2410-5360_2410-5359insG
NM_001105528.4:c.2524-5360_2524-5359insG MANE Select	NP_001098998.1:n.2524-5360_2524-5359insG