Canonical Allele Identifier: CA2154900493
Gene: CCDC88C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91272811C= , CM000676.2:g.91272811C= GRCh38
NC_000014.8:g.91739155C= , CM000676.1:g.91739155C= GRCh37
NC_000014.7:g.90808908C= NCBI36
NG_033118.1:g.150034G=
NG_033118.2:g.150034G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.5901G= MANE Select ENSP00000374507.6:p.Gly1967=
ENST00000331194.8:c.1335G= ENSP00000330332.8:p.Gly445=
ENST00000389857.10:c.5901G= ENSP00000374507.6:p.Gly1967=
ENST00000556726.5:c.2129G=
NM_001080414.3:c.5901G= NP_001073883.2:p.Gly1967=
XM_011536796.1:c.5793G= XP_011535098.1:p.Gly1931=
XM_011536796.2:c.5793G= XP_011535098.1:p.Gly1931=
XM_017021336.1:c.2982G= XP_016876825.1:p.Gly994=
NM_001080414.4:c.5901G= MANE Select NP_001073883.2:p.Gly1967=