Canonical Allele Identifier: CA2154902361

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273435_91273439delinsCTCAG , CM000676.2:g.91273435_91273439delinsCTCAG	GRCh38
NC_000014.8:g.91739779_91739783delinsCTCAG , CM000676.1:g.91739779_91739783delinsCTCAG	GRCh37
NC_000014.7:g.90809532_90809536delinsCTCAG	NCBI36
NG_033118.1:g.149406_149410delinsCTGAG
NG_033118.2:g.149406_149410delinsCTGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5273_5277delinsCTGAG MANE Select	ENSP00000374507.6:p.Thr1758=
ENST00000331194.8:c.845_849delinsCTGAG	ENSP00000330332.8:p.Thr282=
ENST00000389857.10:c.5273_5277delinsCTGAG	ENSP00000374507.6:p.Thr1758=
ENST00000556726.5:c.1501_1505delinsCTGAG
NM_001080414.3:c.5273_5277delinsCTGAG	NP_001073883.2:p.Thr1758=
XM_011536796.1:c.5165_5169delinsCTGAG	XP_011535098.1:p.Thr1722=
XM_011536796.2:c.5165_5169delinsCTGAG	XP_011535098.1:p.Thr1722=
XM_017021336.1:c.2354_2358delinsCTGAG	XP_016876825.1:p.Thr785=
NM_001080414.4:c.5273_5277delinsCTGAG MANE Select	NP_001073883.2:p.Thr1758=