Canonical Allele Identifier: CA2154912640
Gene: CCDC88C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91338068C= , CM000676.2:g.91338068C= GRCh38
NC_000014.8:g.91804412C= , CM000676.1:g.91804412C= GRCh37
NC_000014.7:g.90874165C= NCBI36
NG_033118.1:g.84777G=
NG_033118.2:g.84777G=

Transcript Alleles

HGVS Amino-acid change
ENST00000389857.11:c.987G= MANE Select ENSP00000374507.6:p.Glu329=
ENST00000389857.10:c.987G= ENSP00000374507.6:p.Glu329=
ENST00000554051.1:n.464G=
NM_001080414.3:c.987G= NP_001073883.2:p.Glu329=
XM_005267691.3:c.987G= XP_005267748.1:p.Glu329=
XM_011536796.1:c.879G= XP_011535098.1:p.Glu293=
XR_429316.2:n.1115G=
XR_943459.1:n.1115G=
XM_005267691.5:c.987G= XP_005267748.1:p.Glu329=
XM_011536796.2:c.879G= XP_011535098.1:p.Glu293=
XM_017021335.2:c.987G= XP_016876824.1:p.Glu329=
XM_017021337.2:c.987G= XP_016876826.1:p.Glu329=
XR_429316.4:n.1113G=
NM_001080414.4:c.987G= MANE Select NP_001073883.2:p.Glu329=