Canonical Allele Identifier: CA7309460
Community Standard Title: NM_001080414.4(CCDC88C):c.3097G>A (p.Ala1033Thr)
Gene: CCDC88C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91307136C>T , CM000676.2:g.91307136C>T GRCh38
NC_000014.8:g.91773480C>T , CM000676.1:g.91773480C>T GRCh37
NC_000014.7:g.90843233C>T NCBI36
NG_033118.1:g.115709G>A
NG_033118.2:g.115709G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001080414.4:c.3097G>A MANE Select NP_001073883.2:p.Ala1033Thr
ENST00000389857.11:c.3097G>A MANE Select ENSP00000374507.6:p.Ala1033Thr
NM_001080414.3:c.3097G>A NP_001073883.2:p.Ala1033Thr
ENST00000389857.10:c.3097G>A ENSP00000374507.6:p.Ala1033Thr
XM_005267691.3:c.3097G>A XP_005267748.1:p.Ala1033Thr
XM_005267691.5:c.3097G>A XP_005267748.1:p.Ala1033Thr
XM_011536796.1:c.2989G>A XP_011535098.1:p.Ala997Thr
XM_011536796.2:c.2989G>A XP_011535098.1:p.Ala997Thr
XM_017021335.2:c.3097G>A XP_016876824.1:p.Ala1033Thr
XM_017021336.1:c.178G>A XP_016876825.1:p.Ala60Thr
XR_429316.2:n.3225G>A
XR_429316.4:n.3223G>A
XR_943459.1:n.3225G>A