Canonical Allele Identifier: CA2154901791
Gene: CCDC88C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91306205_91306210delinsGCTTTC , CM000676.2:g.91306205_91306210delinsGCTTTC GRCh38
NC_000014.8:g.91772549_91772554delinsGCTTTC , CM000676.1:g.91772549_91772554delinsGCTTTC GRCh37
NC_000014.7:g.90842302_90842307delinsGCTTTC NCBI36
NG_033118.1:g.116635_116640delinsGAAAGC
NG_033118.2:g.116635_116640delinsGAAAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.3196-284_3196-279delinsGAAAGC MANE Select ENSP00000374507.6:n.3196-284_3196-279delinsGAAAGC
ENST00000389857.10:c.3196-284_3196-279delinsGAAAGC ENSP00000374507.6:n.3196-284_3196-279delinsGAAAGC
NM_001080414.3:c.3196-284_3196-279delinsGAAAGC NP_001073883.2:n.3196-284_3196-279delinsGAAAGC
XM_005267691.3:c.3196-284_3196-279delinsGAAAGC XP_005267748.1:n.3196-284_3196-279delinsGAAAGC
XM_011536796.1:c.3088-284_3088-279delinsGAAAGC XP_011535098.1:n.3088-284_3088-279delinsGAAAGC
XR_429316.2:n.3324-284_3324-279delinsGAAAGC
XR_943459.1:n.3324-284_3324-279delinsGAAAGC
XM_005267691.5:c.3196-284_3196-279delinsGAAAGC XP_005267748.1:n.3196-284_3196-279delinsGAAAGC
XM_011536796.2:c.3088-284_3088-279delinsGAAAGC XP_011535098.1:n.3088-284_3088-279delinsGAAAGC
XM_017021335.2:c.3196-284_3196-279delinsGAAAGC XP_016876824.1:n.3196-284_3196-279delinsGAAAGC
XM_017021336.1:c.277-284_277-279delinsGAAAGC XP_016876825.1:n.277-284_277-279delinsGAAAGC
XR_429316.4:n.3322-284_3322-279delinsGAAAGC
NM_001080414.4:c.3196-284_3196-279delinsGAAAGC MANE Select NP_001073883.2:n.3196-284_3196-279delinsGAAAGC