Canonical Allele Identifier: CA2154912584

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91337970_91337971delinsGC , CM000676.2:g.91337970_91337971delinsGC	GRCh38
NC_000014.8:g.91804314_91804315delinsGC , CM000676.1:g.91804314_91804315delinsGC	GRCh37
NC_000014.7:g.90874067_90874068delinsGC	NCBI36
NG_033118.1:g.84874_84875delinsGC
NG_033118.2:g.84874_84875delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.1050+34_1050+35delinsGC MANE Select	ENSP00000374507.6:n.1050+34_1050+35delinsGC
ENST00000389857.10:c.1050+34_1050+35delinsGC	ENSP00000374507.6:n.1050+34_1050+35delinsGC
NM_001080414.3:c.1050+34_1050+35delinsGC	NP_001073883.2:n.1050+34_1050+35delinsGC
XM_005267691.3:c.1050+34_1050+35delinsGC	XP_005267748.1:n.1050+34_1050+35delinsGC
XM_011536796.1:c.942+34_942+35delinsGC	XP_011535098.1:n.942+34_942+35delinsGC
XR_429316.2:n.1178+34_1178+35delinsGC
XR_943459.1:n.1178+34_1178+35delinsGC
XM_005267691.5:c.1050+34_1050+35delinsGC	XP_005267748.1:n.1050+34_1050+35delinsGC
XM_011536796.2:c.942+34_942+35delinsGC	XP_011535098.1:n.942+34_942+35delinsGC
XM_017021335.2:c.1050+34_1050+35delinsGC	XP_016876824.1:n.1050+34_1050+35delinsGC
XM_017021337.2:c.1050+34_1050+35delinsGC	XP_016876826.1:n.1050+34_1050+35delinsGC
XR_429316.4:n.1176+34_1176+35delinsGC
NM_001080414.4:c.1050+34_1050+35delinsGC MANE Select	NP_001073883.2:n.1050+34_1050+35delinsGC