Canonical Allele Identifier: CA2154902360

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273435C= , CM000676.2:g.91273435C=	GRCh38
NC_000014.8:g.91739779C= , CM000676.1:g.91739779C=	GRCh37
NC_000014.7:g.90809532C=	NCBI36
NG_033118.1:g.149410G=
NG_033118.2:g.149410G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.5277G= MANE Select	ENSP00000374507.6:p.Glu1759=
ENST00000331194.8:c.849G=	ENSP00000330332.8:p.Glu283=
ENST00000389857.10:c.5277G=	ENSP00000374507.6:p.Glu1759=
ENST00000556726.5:c.1505G=
NM_001080414.3:c.5277G=	NP_001073883.2:p.Glu1759=
XM_011536796.1:c.5169G=	XP_011535098.1:p.Glu1723=
XM_011536796.2:c.5169G=	XP_011535098.1:p.Glu1723=
XM_017021336.1:c.2358G=	XP_016876825.1:p.Glu786=
NM_001080414.4:c.5277G= MANE Select	NP_001073883.2:p.Glu1759=