Canonical Allele Identifier: CA2154902721

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273578G= , CM000676.2:g.91273578G=	GRCh38
NC_000014.8:g.91739922G= , CM000676.1:g.91739922G=	GRCh37
NC_000014.7:g.90809675G=	NCBI36
NG_033118.1:g.149267C=
NG_033118.2:g.149267C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5134C= MANE Select	ENSP00000374507.6:p.Gln1712=
ENST00000331194.8:c.706C=	ENSP00000330332.8:p.Gln236=
ENST00000334448.5:n.946C=
ENST00000389857.10:c.5134C=	ENSP00000374507.6:p.Gln1712=
ENST00000556726.5:c.1362C=
NM_001080414.3:c.5134C=	NP_001073883.2:p.Gln1712=
XM_011536796.1:c.5026C=	XP_011535098.1:p.Gln1676=
XR_429316.2:n.5409C=
XM_011536796.2:c.5026C=	XP_011535098.1:p.Gln1676=
XM_017021336.1:c.2215C=	XP_016876825.1:p.Gln739=
XR_429316.4:n.5407C=
NM_001080414.4:c.5134C= MANE Select	NP_001073883.2:p.Gln1712=