Canonical Allele Identifier: CA2154899687

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272418_91272420delinsCAG , CM000676.2:g.91272418_91272420delinsCAG	GRCh38
NC_000014.8:g.91738762_91738764delinsCAG , CM000676.1:g.91738762_91738764delinsCAG	GRCh37
NC_000014.7:g.90808515_90808517delinsCAG	NCBI36
NG_033118.1:g.150425_150427delinsCTG
NG_033118.2:g.150425_150427delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.*205_*207delinsCTG MANE Select	ENSP00000374507.6:n.*205_*207delinsCTG
ENST00000331194.8:c.*205_*207delinsCTG	ENSP00000330332.8:n.*205_*207delinsCTG
ENST00000389857.10:c.*205_*207delinsCTG	ENSP00000374507.6:n.*205_*207delinsCTG
ENST00000556726.5:c.2520_2522delinsCTG
NM_001080414.3:c.*205_*207delinsCTG	NP_001073883.2:n.*205_*207delinsCTG
XM_011536796.1:c.*205_*207delinsCTG	XP_011535098.1:n.*205_*207delinsCTG
XM_011536796.2:c.*205_*207delinsCTG	XP_011535098.1:n.*205_*207delinsCTG
XM_017021336.1:c.*205_*207delinsCTG	XP_016876825.1:n.*205_*207delinsCTG
NM_001080414.4:c.*205_*207delinsCTG MANE Select	NP_001073883.2:n.*205_*207delinsCTG