Canonical Allele Identifier: CA2154899832

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272553_91272554delinsCA , CM000676.2:g.91272553_91272554delinsCA	GRCh38
NC_000014.8:g.91738897_91738898delinsCA , CM000676.1:g.91738897_91738898delinsCA	GRCh37
NC_000014.7:g.90808650_90808651delinsCA	NCBI36
NG_033118.1:g.150291_150292delinsTG
NG_033118.2:g.150291_150292delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.*71_*72delinsTG MANE Select	ENSP00000374507.6:n.*71_*72delinsTG
ENST00000331194.8:c.*71_*72delinsTG	ENSP00000330332.8:n.*71_*72delinsTG
ENST00000389857.10:c.*71_*72delinsTG	ENSP00000374507.6:n.*71_*72delinsTG
ENST00000556726.5:c.2386_2387delinsTG
NM_001080414.3:c.*71_*72delinsTG	NP_001073883.2:n.*71_*72delinsTG
XM_011536796.1:c.*71_*72delinsTG	XP_011535098.1:n.*71_*72delinsTG
XM_011536796.2:c.*71_*72delinsTG	XP_011535098.1:n.*71_*72delinsTG
XM_017021336.1:c.*71_*72delinsTG	XP_016876825.1:n.*71_*72delinsTG
NM_001080414.4:c.*71_*72delinsTG MANE Select	NP_001073883.2:n.*71_*72delinsTG