Canonical Allele Identifier: CA7309836
Community Standard Title: NM_001080414.4(CCDC88C):c.1702C>T (p.Arg568Ter)
Gene: CCDC88C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91314114G>A , CM000676.2:g.91314114G>A GRCh38
NC_000014.8:g.91780458G>A , CM000676.1:g.91780458G>A GRCh37
NC_000014.7:g.90850211G>A NCBI36
NG_033118.1:g.108731C>T
NG_033118.2:g.108731C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001080414.4:c.1702C>T MANE Select NP_001073883.2:p.Arg568Ter
ENST00000389857.11:c.1702C>T MANE Select ENSP00000374507.6:p.Arg568Ter
NM_001080414.3:c.1702C>T NP_001073883.2:p.Arg568Ter
ENST00000389857.10:c.1702C>T ENSP00000374507.6:p.Arg568Ter
ENST00000557507.1:n.258C>T
XM_005267691.3:c.1702C>T XP_005267748.1:p.Arg568Ter
XM_005267691.5:c.1702C>T XP_005267748.1:p.Arg568Ter
XM_011536796.1:c.1594C>T XP_011535098.1:p.Arg532Ter
XM_011536796.2:c.1594C>T XP_011535098.1:p.Arg532Ter
XM_017021335.2:c.1702C>T XP_016876824.1:p.Arg568Ter
XM_017021337.2:c.1702C>T XP_016876826.1:p.Arg568Ter
XR_429316.2:n.1830C>T
XR_429316.4:n.1828C>T
XR_943459.1:n.1830C>T