Canonical Allele Identifier: CA2154899835

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272554_91272556delinsAAG , CM000676.2:g.91272554_91272556delinsAAG	GRCh38
NC_000014.8:g.91738898_91738900delinsAAG , CM000676.1:g.91738898_91738900delinsAAG	GRCh37
NC_000014.7:g.90808651_90808653delinsAAG	NCBI36
NG_033118.1:g.150289_150291delinsCTT
NG_033118.2:g.150289_150291delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.*69_*71delinsCTT MANE Select	ENSP00000374507.6:n.*69_*71delinsCTT
ENST00000331194.8:c.*69_*71delinsCTT	ENSP00000330332.8:n.*69_*71delinsCTT
ENST00000389857.10:c.*69_*71delinsCTT	ENSP00000374507.6:n.*69_*71delinsCTT
ENST00000556726.5:c.2384_2386delinsCTT
NM_001080414.3:c.*69_*71delinsCTT	NP_001073883.2:n.*69_*71delinsCTT
XM_011536796.1:c.*69_*71delinsCTT	XP_011535098.1:n.*69_*71delinsCTT
XM_011536796.2:c.*69_*71delinsCTT	XP_011535098.1:n.*69_*71delinsCTT
XM_017021336.1:c.*69_*71delinsCTT	XP_016876825.1:n.*69_*71delinsCTT
NM_001080414.4:c.*69_*71delinsCTT MANE Select	NP_001073883.2:n.*69_*71delinsCTT