Canonical Allele Identifier: CA2154900520

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272820C= , CM000676.2:g.91272820C=	GRCh38
NC_000014.8:g.91739164C= , CM000676.1:g.91739164C=	GRCh37
NC_000014.7:g.90808917C=	NCBI36
NG_033118.1:g.150025G=
NG_033118.2:g.150025G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5892G= MANE Select	ENSP00000374507.6:p.Glu1964=
ENST00000331194.8:c.1326G=	ENSP00000330332.8:p.Glu442=
ENST00000389857.10:c.5892G=	ENSP00000374507.6:p.Glu1964=
ENST00000556726.5:c.2120G=
NM_001080414.3:c.5892G=	NP_001073883.2:p.Glu1964=
XM_011536796.1:c.5784G=	XP_011535098.1:p.Glu1928=
XM_011536796.2:c.5784G=	XP_011535098.1:p.Glu1928=
XM_017021336.1:c.2973G=	XP_016876825.1:p.Glu991=
NM_001080414.4:c.5892G= MANE Select	NP_001073883.2:p.Glu1964=