Canonical Allele Identifier: CA2154879055

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91313564C= , CM000676.2:g.91313564C=	GRCh38
NC_000014.8:g.91779908C= , CM000676.1:g.91779908C=	GRCh37
NC_000014.7:g.90849661C=	NCBI36
NG_033118.1:g.109281G=
NG_033118.2:g.109281G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.2252G= MANE Select	ENSP00000374507.6:p.Gly751=
ENST00000389857.10:c.2252G=	ENSP00000374507.6:p.Gly751=
NM_001080414.3:c.2252G=	NP_001073883.2:p.Gly751=
XM_005267691.3:c.2252G=	XP_005267748.1:p.Gly751=
XM_011536796.1:c.2144G=	XP_011535098.1:p.Gly715=
XR_429316.2:n.2380G=
XR_943459.1:n.2380G=
XM_005267691.5:c.2252G=	XP_005267748.1:p.Gly751=
XM_011536796.2:c.2144G=	XP_011535098.1:p.Gly715=
XM_017021335.2:c.2252G=	XP_016876824.1:p.Gly751=
XM_017021337.2:c.2252G=	XP_016876826.1:p.Gly751=
XR_429316.4:n.2378G=
NM_001080414.4:c.2252G= MANE Select	NP_001073883.2:p.Gly751=