Canonical Allele Identifier: CA2154902925

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273663_91273664delinsAG , CM000676.2:g.91273663_91273664delinsAG	GRCh38
NC_000014.8:g.91740007_91740008delinsAG , CM000676.1:g.91740007_91740008delinsAG	GRCh37
NC_000014.7:g.90809760_90809761delinsAG	NCBI36
NG_033118.1:g.149181_149182delinsCT
NG_033118.2:g.149181_149182delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5059-11_5059-10delinsCT MANE Select	ENSP00000374507.6:n.5059-11_5059-10delinsCT
ENST00000331194.8:c.631-11_631-10delinsCT	ENSP00000330332.8:n.631-11_631-10delinsCT
ENST00000334448.5:n.871-11_871-10delinsCT
ENST00000389857.10:c.5059-11_5059-10delinsCT	ENSP00000374507.6:n.5059-11_5059-10delinsCT
ENST00000556726.5:c.1287-11_1287-10delinsCT
NM_001080414.3:c.5059-11_5059-10delinsCT	NP_001073883.2:n.5059-11_5059-10delinsCT
XM_011536796.1:c.4951-11_4951-10delinsCT	XP_011535098.1:n.4951-11_4951-10delinsCT
XR_429316.2:n.5334-11_5334-10delinsCT
XM_011536796.2:c.4951-11_4951-10delinsCT	XP_011535098.1:n.4951-11_4951-10delinsCT
XM_017021336.1:c.2140-11_2140-10delinsCT	XP_016876825.1:n.2140-11_2140-10delinsCT
XR_429316.4:n.5332-11_5332-10delinsCT
NM_001080414.4:c.5059-11_5059-10delinsCT MANE Select	NP_001073883.2:n.5059-11_5059-10delinsCT