Canonical Allele Identifier: CA2154902754

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273602T= , CM000676.2:g.91273602T=	GRCh38
NC_000014.8:g.91739946T= , CM000676.1:g.91739946T=	GRCh37
NC_000014.7:g.90809699T=	NCBI36
NG_033118.1:g.149243A=
NG_033118.2:g.149243A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5110A= MANE Select	ENSP00000374507.6:p.Ser1704=
ENST00000331194.8:c.682A=	ENSP00000330332.8:p.Ser228=
ENST00000334448.5:n.922A=
ENST00000389857.10:c.5110A=	ENSP00000374507.6:p.Ser1704=
ENST00000556726.5:c.1338A=
NM_001080414.3:c.5110A=	NP_001073883.2:p.Ser1704=
XM_011536796.1:c.5002A=	XP_011535098.1:p.Ser1668=
XR_429316.2:n.5385A=
XM_011536796.2:c.5002A=	XP_011535098.1:p.Ser1668=
XM_017021336.1:c.2191A=	XP_016876825.1:p.Ser731=
XR_429316.4:n.5383A=
NM_001080414.4:c.5110A= MANE Select	NP_001073883.2:p.Ser1704=