Canonical Allele Identifier: CA2154909484
Gene: CCDC88C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91279302C= , CM000676.2:g.91279302C= GRCh38
NC_000014.8:g.91745646C= , CM000676.1:g.91745646C= GRCh37
NC_000014.7:g.90815399C= NCBI36
NG_033118.1:g.143543G=
NG_033118.2:g.143543G=

Transcript Alleles

HGVS Amino-acid change
ENST00000389857.11:c.4704G= MANE Select ENSP00000374507.6:p.Ser1568=
ENST00000331194.8:c.276G= ENSP00000330332.8:p.Ser92=
ENST00000334448.5:n.516G=
ENST00000389857.10:c.4704G= ENSP00000374507.6:p.Ser1568=
ENST00000556726.5:c.932G=
ENST00000557455.1:n.676G=
NM_001080414.3:c.4704G= NP_001073883.2:p.Ser1568=
XM_011536796.1:c.4596G= XP_011535098.1:p.Ser1532=
XR_429316.2:n.4979G=
XM_011536796.2:c.4596G= XP_011535098.1:p.Ser1532=
XM_017021336.1:c.1785G= XP_016876825.1:p.Ser595=
XR_429316.4:n.4977G=
NM_001080414.4:c.4704G= MANE Select NP_001073883.2:p.Ser1568=