Canonical Allele Identifier: CA2154878363

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91313149C= , CM000676.2:g.91313149C=	GRCh38
NC_000014.8:g.91779493C= , CM000676.1:g.91779493C=	GRCh37
NC_000014.7:g.90849246C=	NCBI36
NG_033118.1:g.109696G=
NG_033118.2:g.109696G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.2667G= MANE Select	ENSP00000374507.6:p.Leu889=
ENST00000389857.10:c.2667G=	ENSP00000374507.6:p.Leu889=
NM_001080414.3:c.2667G=	NP_001073883.2:p.Leu889=
XM_005267691.3:c.2667G=	XP_005267748.1:p.Leu889=
XM_011536796.1:c.2559G=	XP_011535098.1:p.Leu853=
XR_429316.2:n.2795G=
XR_943459.1:n.2795G=
XM_005267691.5:c.2667G=	XP_005267748.1:p.Leu889=
XM_011536796.2:c.2559G=	XP_011535098.1:p.Leu853=
XM_017021335.2:c.2667G=	XP_016876824.1:p.Leu889=
XM_017021336.1:c.-125G=	XP_016876825.1:n.-125G=
XM_017021337.2:c.2667G=	XP_016876826.1:p.Leu889=
XR_429316.4:n.2793G=
NM_001080414.4:c.2667G= MANE Select	NP_001073883.2:p.Leu889=