Canonical Allele Identifier: CA2154910488

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91281492G= , CM000676.2:g.91281492G=	GRCh38
NC_000014.8:g.91747836G= , CM000676.1:g.91747836G=	GRCh37
NC_000014.7:g.90817589G=	NCBI36
NG_033118.1:g.141353C=
NG_033118.2:g.141353C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.4664C= MANE Select	ENSP00000374507.6:p.Ser1555=
ENST00000331194.8:c.236C=	ENSP00000330332.8:p.Ser79=
ENST00000334448.5:n.329C=
ENST00000389857.10:c.4664C=	ENSP00000374507.6:p.Ser1555=
ENST00000556726.5:c.892C=
NM_001080414.3:c.4664C=	NP_001073883.2:p.Ser1555=
XM_011536796.1:c.4556C=	XP_011535098.1:p.Ser1519=
XR_429316.2:n.4792C=
XR_943459.1:n.4792C=
XM_011536796.2:c.4556C=	XP_011535098.1:p.Ser1519=
XM_017021335.2:c.4664C=	XP_016876824.1:p.Ser1555=
XM_017021336.1:c.1745C=	XP_016876825.1:p.Ser582=
XR_429316.4:n.4790C=
NM_001080414.4:c.4664C= MANE Select	NP_001073883.2:p.Ser1555=