Canonical Allele Identifier: CA2154879029

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91313544C= , CM000676.2:g.91313544C=	GRCh38
NC_000014.8:g.91779888C= , CM000676.1:g.91779888C=	GRCh37
NC_000014.7:g.90849641C=	NCBI36
NG_033118.1:g.109301G=
NG_033118.2:g.109301G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.2272G= MANE Select	ENSP00000374507.6:p.Glu758=
ENST00000389857.10:c.2272G=	ENSP00000374507.6:p.Glu758=
NM_001080414.3:c.2272G=	NP_001073883.2:p.Glu758=
XM_005267691.3:c.2272G=	XP_005267748.1:p.Glu758=
XM_011536796.1:c.2164G=	XP_011535098.1:p.Glu722=
XR_429316.2:n.2400G=
XR_943459.1:n.2400G=
XM_005267691.5:c.2272G=	XP_005267748.1:p.Glu758=
XM_011536796.2:c.2164G=	XP_011535098.1:p.Glu722=
XM_017021335.2:c.2272G=	XP_016876824.1:p.Glu758=
XM_017021337.2:c.2272G=	XP_016876826.1:p.Glu758=
XR_429316.4:n.2398G=
NM_001080414.4:c.2272G= MANE Select	NP_001073883.2:p.Glu758=