Canonical Allele Identifier: CA2154888449
Gene: CCDC88C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91297280G= , CM000676.2:g.91297280G= GRCh38
NC_000014.8:g.91763624G= , CM000676.1:g.91763624G= GRCh37
NC_000014.7:g.90833377G= NCBI36
NG_033118.1:g.125565C=
NG_033118.2:g.125565C=

Transcript Alleles

HGVS Amino-acid change
ENST00000389857.11:c.3966+25C= MANE Select ENSP00000374507.6:n.3966+25C=
ENST00000389857.10:c.3966+25C= ENSP00000374507.6:n.3966+25C=
NM_001080414.3:c.3966+25C= NP_001073883.2:n.3966+25C=
XM_005267691.3:c.3966+25C= XP_005267748.1:n.3966+25C=
XM_011536796.1:c.3858+25C= XP_011535098.1:n.3858+25C=
XR_429316.2:n.4094+25C=
XR_943459.1:n.4094+25C=
XM_005267691.5:c.3966+25C= XP_005267748.1:n.3966+25C=
XM_011536796.2:c.3858+25C= XP_011535098.1:n.3858+25C=
XM_017021335.2:c.3966+25C= XP_016876824.1:n.3966+25C=
XM_017021336.1:c.1047+25C= XP_016876825.1:n.1047+25C=
XR_429316.4:n.4092+25C=
NM_001080414.4:c.3966+25C= MANE Select NP_001073883.2:n.3966+25C=