Canonical Allele Identifier: CA2154888499

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91297313G= , CM000676.2:g.91297313G=	GRCh38
NC_000014.8:g.91763657G= , CM000676.1:g.91763657G=	GRCh37
NC_000014.7:g.90833410G=	NCBI36
NG_033118.1:g.125532C=
NG_033118.2:g.125532C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.3958C= MANE Select	ENSP00000374507.6:p.His1320=
ENST00000389857.10:c.3958C=	ENSP00000374507.6:p.His1320=
NM_001080414.3:c.3958C=	NP_001073883.2:p.His1320=
XM_005267691.3:c.3958C=	XP_005267748.1:p.His1320=
XM_011536796.1:c.3850C=	XP_011535098.1:p.His1284=
XR_429316.2:n.4086C=
XR_943459.1:n.4086C=
XM_005267691.5:c.3958C=	XP_005267748.1:p.His1320=
XM_011536796.2:c.3850C=	XP_011535098.1:p.His1284=
XM_017021335.2:c.3958C=	XP_016876824.1:p.His1320=
XM_017021336.1:c.1039C=	XP_016876825.1:p.His347=
XR_429316.4:n.4084C=
NM_001080414.4:c.3958C= MANE Select	NP_001073883.2:p.His1320=