Canonical Allele Identifier: CA2154912668
Gene: CCDC88C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91338124A= , CM000676.2:g.91338124A= GRCh38
NC_000014.8:g.91804468A= , CM000676.1:g.91804468A= GRCh37
NC_000014.7:g.90874221A= NCBI36
NG_033118.1:g.84721T=
NG_033118.2:g.84721T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.931T= MANE Select ENSP00000374507.6:p.Tyr311=
ENST00000389857.10:c.931T= ENSP00000374507.6:p.Tyr311=
ENST00000554051.1:n.408T=
NM_001080414.3:c.931T= NP_001073883.2:p.Tyr311=
XM_005267691.3:c.931T= XP_005267748.1:p.Tyr311=
XM_011536796.1:c.823T= XP_011535098.1:p.Tyr275=
XR_429316.2:n.1059T=
XR_943459.1:n.1059T=
XM_005267691.5:c.931T= XP_005267748.1:p.Tyr311=
XM_011536796.2:c.823T= XP_011535098.1:p.Tyr275=
XM_017021335.2:c.931T= XP_016876824.1:p.Tyr311=
XM_017021337.2:c.931T= XP_016876826.1:p.Tyr311=
XR_429316.4:n.1057T=
NM_001080414.4:c.931T= MANE Select NP_001073883.2:p.Tyr311=