Canonical Allele Identifier: CA2154912632
Gene: CCDC88C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91338046C= , CM000676.2:g.91338046C= GRCh38
NC_000014.8:g.91804390C= , CM000676.1:g.91804390C= GRCh37
NC_000014.7:g.90874143C= NCBI36
NG_033118.1:g.84799G=
NG_033118.2:g.84799G=

Transcript Alleles

HGVS Amino-acid change
ENST00000389857.11:c.1009G= MANE Select ENSP00000374507.6:p.Glu337=
ENST00000389857.10:c.1009G= ENSP00000374507.6:p.Glu337=
NM_001080414.3:c.1009G= NP_001073883.2:p.Glu337=
XM_005267691.3:c.1009G= XP_005267748.1:p.Glu337=
XM_011536796.1:c.901G= XP_011535098.1:p.Glu301=
XR_429316.2:n.1137G=
XR_943459.1:n.1137G=
XM_005267691.5:c.1009G= XP_005267748.1:p.Glu337=
XM_011536796.2:c.901G= XP_011535098.1:p.Glu301=
XM_017021335.2:c.1009G= XP_016876824.1:p.Glu337=
XM_017021337.2:c.1009G= XP_016876826.1:p.Glu337=
XR_429316.4:n.1135G=
NM_001080414.4:c.1009G= MANE Select NP_001073883.2:p.Glu337=