Canonical Allele Identifier: CA2154909394

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91279111_91279112delinsGC , CM000676.2:g.91279111_91279112delinsGC	GRCh38
NC_000014.8:g.91745455_91745456delinsGC , CM000676.1:g.91745455_91745456delinsGC	GRCh37
NC_000014.7:g.90815208_90815209delinsGC	NCBI36
NG_033118.1:g.143733_143734delinsGC
NG_033118.2:g.143733_143734delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.4768+126_4768+127delinsGC MANE Select	ENSP00000374507.6:n.4768+126_4768+127delinsGC
ENST00000331194.8:c.340+126_340+127delinsGC	ENSP00000330332.8:n.340+126_340+127delinsGC
ENST00000334448.5:n.580+126_580+127delinsGC
ENST00000389857.10:c.4768+126_4768+127delinsGC	ENSP00000374507.6:n.4768+126_4768+127delinsGC
ENST00000556726.5:c.996+126_996+127delinsGC
ENST00000557455.1:n.740+126_740+127delinsGC
NM_001080414.3:c.4768+126_4768+127delinsGC	NP_001073883.2:n.4768+126_4768+127delinsGC
XM_011536796.1:c.4660+126_4660+127delinsGC	XP_011535098.1:n.4660+126_4660+127delinsGC
XR_429316.2:n.5043+126_5043+127delinsGC
XM_011536796.2:c.4660+126_4660+127delinsGC	XP_011535098.1:n.4660+126_4660+127delinsGC
XM_017021336.1:c.1849+126_1849+127delinsGC	XP_016876825.1:n.1849+126_1849+127delinsGC
XR_429316.4:n.5041+126_5041+127delinsGC
NM_001080414.4:c.4768+126_4768+127delinsGC MANE Select	NP_001073883.2:n.4768+126_4768+127delinsGC