Canonical Allele Identifier: CA2154912691
Gene: CCDC88C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91338174G= , CM000676.2:g.91338174G= GRCh38
NC_000014.8:g.91804518G= , CM000676.1:g.91804518G= GRCh37
NC_000014.7:g.90874271G= NCBI36
NG_033118.1:g.84671C=
NG_033118.2:g.84671C=

Transcript Alleles

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