Canonical Allele Identifier: CA2154910487

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91281491G= , CM000676.2:g.91281491G=	GRCh38
NC_000014.8:g.91747835G= , CM000676.1:g.91747835G=	GRCh37
NC_000014.7:g.90817588G=	NCBI36
NG_033118.1:g.141354C=
NG_033118.2:g.141354C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.4665C= MANE Select	ENSP00000374507.6:p.Ser1555=
ENST00000331194.8:c.237C=	ENSP00000330332.8:p.Ser79=
ENST00000334448.5:n.330C=
ENST00000389857.10:c.4665C=	ENSP00000374507.6:p.Ser1555=
ENST00000556726.5:c.893C=
NM_001080414.3:c.4665C=	NP_001073883.2:p.Ser1555=
XM_011536796.1:c.4557C=	XP_011535098.1:p.Ser1519=
XR_429316.2:n.4793C=
XR_943459.1:n.4793C=
XM_011536796.2:c.4557C=	XP_011535098.1:p.Ser1519=
XM_017021335.2:c.4665C=	XP_016876824.1:p.Ser1555=
XM_017021336.1:c.1746C=	XP_016876825.1:p.Ser582=
XR_429316.4:n.4791C=
NM_001080414.4:c.4665C= MANE Select	NP_001073883.2:p.Ser1555=