Canonical Allele Identifier: CA2154902774

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273619T= , CM000676.2:g.91273619T=	GRCh38
NC_000014.8:g.91739963T= , CM000676.1:g.91739963T=	GRCh37
NC_000014.7:g.90809716T=	NCBI36
NG_033118.1:g.149226A=
NG_033118.2:g.149226A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5093A= MANE Select	ENSP00000374507.6:p.Asp1698=
ENST00000331194.8:c.665A=	ENSP00000330332.8:p.Asp222=
ENST00000334448.5:n.905A=
ENST00000389857.10:c.5093A=	ENSP00000374507.6:p.Asp1698=
ENST00000556726.5:c.1321A=
NM_001080414.3:c.5093A=	NP_001073883.2:p.Asp1698=
XM_011536796.1:c.4985A=	XP_011535098.1:p.Asp1662=
XR_429316.2:n.5368A=
XM_011536796.2:c.4985A=	XP_011535098.1:p.Asp1662=
XM_017021336.1:c.2174A=	XP_016876825.1:p.Asp725=
XR_429316.4:n.5366A=
NM_001080414.4:c.5093A= MANE Select	NP_001073883.2:p.Asp1698=