Canonical Allele Identifier: CA2154912683

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91338146T= , CM000676.2:g.91338146T=	GRCh38
NC_000014.8:g.91804490T= , CM000676.1:g.91804490T=	GRCh37
NC_000014.7:g.90874243T=	NCBI36
NG_033118.1:g.84699A=
NG_033118.2:g.84699A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.909A= MANE Select	ENSP00000374507.6:p.Ala303=
ENST00000389857.10:c.909A=	ENSP00000374507.6:p.Ala303=
ENST00000554051.1:n.386A=
NM_001080414.3:c.909A=	NP_001073883.2:p.Ala303=
XM_005267691.3:c.909A=	XP_005267748.1:p.Ala303=
XM_011536796.1:c.801A=	XP_011535098.1:p.Ala267=
XR_429316.2:n.1037A=
XR_943459.1:n.1037A=
XM_005267691.5:c.909A=	XP_005267748.1:p.Ala303=
XM_011536796.2:c.801A=	XP_011535098.1:p.Ala267=
XM_017021335.2:c.909A=	XP_016876824.1:p.Ala303=
XM_017021337.2:c.909A=	XP_016876826.1:p.Ala303=
XR_429316.4:n.1035A=
NM_001080414.4:c.909A= MANE Select	NP_001073883.2:p.Ala303=