Canonical Allele Identifier: CA2697554099
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 2706818
ClinVar RCV Id: RCV003552171

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91338170G>C , CM000676.2:g.91338170G>C GRCh38
NC_000014.8:g.91804514G>C , CM000676.1:g.91804514G>C GRCh37
NC_000014.7:g.90874267G>C NCBI36
NG_033118.1:g.84675C>G
NG_033118.2:g.84675C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000389857.11:c.892-7C>G MANE Select ENSP00000374507.6:n.892-7C>G
ENST00000389857.10:c.892-7C>G ENSP00000374507.6:n.892-7C>G
ENST00000554051.1:n.369-7C>G
NM_001080414.3:c.892-7C>G NP_001073883.2:n.892-7C>G
XM_005267691.3:c.892-7C>G XP_005267748.1:n.892-7C>G
XM_011536796.1:c.784-7C>G XP_011535098.1:n.784-7C>G
XR_429316.2:n.1020-7C>G
XR_943459.1:n.1020-7C>G
XM_005267691.5:c.892-7C>G XP_005267748.1:n.892-7C>G
XM_011536796.2:c.784-7C>G XP_011535098.1:n.784-7C>G
XM_017021335.2:c.892-7C>G XP_016876824.1:n.892-7C>G
XM_017021337.2:c.892-7C>G XP_016876826.1:n.892-7C>G
XR_429316.4:n.1018-7C>G
NM_001080414.4:c.892-7C>G MANE Select NP_001073883.2:n.892-7C>G