Canonical Allele Identifier: CA2154912693
Gene: CCDC88C HGNC NCBI

Linked Data

dbSNP Id: rs1893140290
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91338179del , CM000676.2:g.91338179del GRCh38
NC_000014.8:g.91804523del , CM000676.1:g.91804523del GRCh37
NC_000014.7:g.90874276del NCBI36
NG_033118.1:g.84668del
NG_033118.2:g.84668del

Transcript Alleles

HGVS Amino-acid change
ENST00000389857.11:c.892-14del MANE Select ENSP00000374507.6:n.892-14del
ENST00000389857.10:c.892-14del ENSP00000374507.6:n.892-14del
ENST00000554051.1:n.369-14del
NM_001080414.3:c.892-14del NP_001073883.2:n.892-14del
XM_005267691.3:c.892-14del XP_005267748.1:n.892-14del
XM_011536796.1:c.784-14del XP_011535098.1:n.784-14del
XR_429316.2:n.1020-14del
XR_943459.1:n.1020-14del
XM_005267691.5:c.892-14del XP_005267748.1:n.892-14del
XM_011536796.2:c.784-14del XP_011535098.1:n.784-14del
XM_017021335.2:c.892-14del XP_016876824.1:n.892-14del
XM_017021337.2:c.892-14del XP_016876826.1:n.892-14del
XR_429316.4:n.1018-14del
NM_001080414.4:c.892-14del MANE Select NP_001073883.2:n.892-14del
Search 100 bp 5'
Search 100 bp 3'