Canonical Allele Identifier: CA2626126831
Gene: CCDC88C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91272411_91272445del , CM000676.2:g.91272411_91272445del GRCh38
NC_000014.8:g.91738755_91738789del , CM000676.1:g.91738755_91738789del GRCh37
NC_000014.7:g.90808508_90808542del NCBI36
NG_033118.1:g.150409_150443del
NG_033118.2:g.150409_150443del

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.*189_*223del MANE Select ENSP00000374507.6:n.*189_*223del
ENST00000331194.8:c.*189_*223del ENSP00000330332.8:n.*189_*223del
ENST00000389857.10:c.*189_*223del ENSP00000374507.6:n.*189_*223del
ENST00000556726.5:c.2504_2538del
NM_001080414.3:c.*189_*223del NP_001073883.2:n.*189_*223del
XM_011536796.1:c.*189_*223del XP_011535098.1:n.*189_*223del
XM_011536796.2:c.*189_*223del XP_011535098.1:n.*189_*223del
XM_017021336.1:c.*189_*223del XP_016876825.1:n.*189_*223del
NM_001080414.4:c.*189_*223del MANE Select NP_001073883.2:n.*189_*223del