Canonical Allele Identifier: CA2154901335

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91305814A= , CM000676.2:g.91305814A=	GRCh38
NC_000014.8:g.91772158A= , CM000676.1:g.91772158A=	GRCh37
NC_000014.7:g.90841911A=	NCBI36
NG_033118.1:g.117031T=
NG_033118.2:g.117031T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.3308T= MANE Select	ENSP00000374507.6:p.Phe1103=
ENST00000389857.10:c.3308T=	ENSP00000374507.6:p.Phe1103=
NM_001080414.3:c.3308T=	NP_001073883.2:p.Phe1103=
XM_005267691.3:c.3308T=	XP_005267748.1:p.Phe1103=
XM_011536796.1:c.3200T=	XP_011535098.1:p.Phe1067=
XR_429316.2:n.3436T=
XR_943459.1:n.3436T=
XM_005267691.5:c.3308T=	XP_005267748.1:p.Phe1103=
XM_011536796.2:c.3200T=	XP_011535098.1:p.Phe1067=
XM_017021335.2:c.3308T=	XP_016876824.1:p.Phe1103=
XM_017021336.1:c.389T=	XP_016876825.1:p.Phe130=
XR_429316.4:n.3434T=
NM_001080414.4:c.3308T= MANE Select	NP_001073883.2:p.Phe1103=