Canonical Allele Identifier: CA2154899783

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272507_91272508delinsGA , CM000676.2:g.91272507_91272508delinsGA	GRCh38
NC_000014.8:g.91738851_91738852delinsGA , CM000676.1:g.91738851_91738852delinsGA	GRCh37
NC_000014.7:g.90808604_90808605delinsGA	NCBI36
NG_033118.1:g.150337_150338delinsTC
NG_033118.2:g.150337_150338delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.*117_*118delinsTC MANE Select	ENSP00000374507.6:n.*117_*118delinsTC
ENST00000331194.8:c.*117_*118delinsTC	ENSP00000330332.8:n.*117_*118delinsTC
ENST00000389857.10:c.*117_*118delinsTC	ENSP00000374507.6:n.*117_*118delinsTC
ENST00000556726.5:c.2432_2433delinsTC
NM_001080414.3:c.*117_*118delinsTC	NP_001073883.2:n.*117_*118delinsTC
XM_011536796.1:c.*117_*118delinsTC	XP_011535098.1:n.*117_*118delinsTC
XM_011536796.2:c.*117_*118delinsTC	XP_011535098.1:n.*117_*118delinsTC
XM_017021336.1:c.*117_*118delinsTC	XP_016876825.1:n.*117_*118delinsTC
NM_001080414.4:c.*117_*118delinsTC MANE Select	NP_001073883.2:n.*117_*118delinsTC