Canonical Allele Identifier: CA2802580900
Gene: CCDC88C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91272340_91272341insA , CM000676.2:g.91272340_91272341insA GRCh38
NC_000014.8:g.91738684_91738685insA , CM000676.1:g.91738684_91738685insA GRCh37
NC_000014.7:g.90808437_90808438insA NCBI36
NG_033118.1:g.150504_150505insT
NG_033118.2:g.150504_150505insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.*284_*285insT MANE Select ENSP00000374507.6:n.*284_*285insT
ENST00000331194.8:c.*284_*285insT ENSP00000330332.8:n.*284_*285insT
ENST00000389857.10:c.*284_*285insT ENSP00000374507.6:n.*284_*285insT
ENST00000556726.5:c.2599_2600insT
NM_001080414.3:c.*284_*285insT NP_001073883.2:n.*284_*285insT
XM_011536796.1:c.*284_*285insT XP_011535098.1:n.*284_*285insT
XM_011536796.2:c.*284_*285insT XP_011535098.1:n.*284_*285insT
XM_017021336.1:c.*284_*285insT XP_016876825.1:n.*284_*285insT
NM_001080414.4:c.*284_*285insT MANE Select NP_001073883.2:n.*284_*285insT