Canonical Allele Identifier: CA2626130283
Gene: CCDC88C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91312988_91312989del , CM000676.2:g.91312988_91312989del GRCh38
NC_000014.8:g.91779332_91779333del , CM000676.1:g.91779332_91779333del GRCh37
NC_000014.7:g.90849085_90849086del NCBI36
NG_033118.1:g.109859_109860del
NG_033118.2:g.109859_109860del

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.2736+94_2736+95del MANE Select ENSP00000374507.6:n.2736+94_2736+95del
ENST00000389857.10:c.2736+94_2736+95del ENSP00000374507.6:n.2736+94_2736+95del
NM_001080414.3:c.2736+94_2736+95del NP_001073883.2:n.2736+94_2736+95del
XM_005267691.3:c.2736+94_2736+95del XP_005267748.1:n.2736+94_2736+95del
XM_011536796.1:c.2628+94_2628+95del XP_011535098.1:n.2628+94_2628+95del
XR_429316.2:n.2864+94_2864+95del
XR_943459.1:n.2864+94_2864+95del
XM_005267691.5:c.2736+94_2736+95del XP_005267748.1:n.2736+94_2736+95del
XM_011536796.2:c.2628+94_2628+95del XP_011535098.1:n.2628+94_2628+95del
XM_017021335.2:c.2736+94_2736+95del XP_016876824.1:n.2736+94_2736+95del
XM_017021336.1:c.-56+94_-56+95del XP_016876825.1:n.-56+94_-56+95del
XM_017021337.2:c.2736+94_2736+95del XP_016876826.1:n.2736+94_2736+95del
XR_429316.4:n.2862+94_2862+95del
NM_001080414.4:c.2736+94_2736+95del MANE Select NP_001073883.2:n.2736+94_2736+95del