Canonical Allele Identifier: CA2294495288

Gene: CCDC178

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.32943528_32943532delinsCTTCA , CM000680.2:g.32943528_32943532delinsCTTCA	GRCh38
NC_000018.9:g.30523492_30523496delinsCTTCA , CM000680.1:g.30523492_30523496delinsCTTCA	GRCh37
NC_000018.8:g.28777490_28777494delinsCTTCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383096.8:c.2524-5441_2524-5437delinsTGAAG MANE Select	ENSP00000372576.3:n.2524-5441_2524-5437delinsTGAAG
ENST00000300227.12:c.2410-5441_2410-5437delinsTGAAG	ENSP00000300227.8:n.2410-5441_2410-5437delinsTGAAG
ENST00000383096.7:c.2524-5441_2524-5437delinsTGAAG	ENSP00000372576.3:n.2524-5441_2524-5437delinsTGAAG
ENST00000403303.5:c.2524-5441_2524-5437delinsTGAAG	ENSP00000385591.1:n.2524-5441_2524-5437delinsTGAAG
ENST00000406524.6:c.2596-5441_2596-5437delinsTGAAG	ENSP00000385867.2:n.2596-5441_2596-5437delinsTGAAG
ENST00000579916.5:c.484-5441_484-5437delinsTGAAG	ENSP00000462153.1:n.484-5441_484-5437delinsTGAAG
ENST00000581524.5:c.1015-5441_1015-5437delinsTGAAG	ENSP00000462651.1:n.1015-5441_1015-5437delinsTGAAG
ENST00000581852.5:c.139-5441_139-5437delinsTGAAG	ENSP00000464295.1:n.139-5441_139-5437delinsTGAAG
ENST00000583930.5:c.2596-5441_2596-5437delinsTGAAG	ENSP00000463254.1:n.2596-5441_2596-5437delinsTGAAG
NM_001105528.1:c.2524-5441_2524-5437delinsTGAAG	NP_001098998.1:n.2524-5441_2524-5437delinsTGAAG
NM_001308126.1:c.2596-5441_2596-5437delinsTGAAG	NP_001295055.1:n.2596-5441_2596-5437delinsTGAAG
NM_198995.2:c.2410-5441_2410-5437delinsTGAAG	NP_945346.2:n.2410-5441_2410-5437delinsTGAAG
XM_011525948.1:c.2524-5441_2524-5437delinsTGAAG	XP_011524250.1:n.2524-5441_2524-5437delinsTGAAG
XM_011525951.1:c.2374-5441_2374-5437delinsTGAAG	XP_011524253.1:n.2374-5441_2374-5437delinsTGAAG
XR_935363.1:n.179+5251_179+5255delinsCTTCA
XM_017025721.1:c.2596-5441_2596-5437delinsTGAAG	XP_016881210.1:n.2596-5441_2596-5437delinsTGAAG
XM_017025722.1:c.2596-5441_2596-5437delinsTGAAG	XP_016881211.1:n.2596-5441_2596-5437delinsTGAAG
XM_017025723.1:c.2596-5441_2596-5437delinsTGAAG	XP_016881212.1:n.2596-5441_2596-5437delinsTGAAG
XM_017025724.1:c.2110-5441_2110-5437delinsTGAAG	XP_016881213.1:n.2110-5441_2110-5437delinsTGAAG
XM_017025725.1:c.2110-5441_2110-5437delinsTGAAG	XP_016881214.1:n.2110-5441_2110-5437delinsTGAAG
XR_001753402.1:n.179+5251_179+5255delinsCTTCA
XR_935363.2:n.179+5251_179+5255delinsCTTCA
XR_935365.2:n.179+5251_179+5255delinsCTTCA
NM_001105528.3:c.2524-5441_2524-5437delinsTGAAG	NP_001098998.1:n.2524-5441_2524-5437delinsTGAAG
NM_001308126.3:c.2596-5441_2596-5437delinsTGAAG	NP_001295055.1:n.2596-5441_2596-5437delinsTGAAG
NM_001371120.1:c.2596-5441_2596-5437delinsTGAAG	NP_001358049.1:n.2596-5441_2596-5437delinsTGAAG
NM_001371121.1:c.2596-5441_2596-5437delinsTGAAG	NP_001358050.1:n.2596-5441_2596-5437delinsTGAAG
NM_198995.3:c.2410-5441_2410-5437delinsTGAAG	NP_945346.2:n.2410-5441_2410-5437delinsTGAAG
NM_001105528.4:c.2524-5441_2524-5437delinsTGAAG MANE Select	NP_001098998.1:n.2524-5441_2524-5437delinsTGAAG