Canonical Allele Identifier: CA2154909543

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91279423C= , CM000676.2:g.91279423C=	GRCh38
NC_000014.8:g.91745767C= , CM000676.1:g.91745767C=	GRCh37
NC_000014.7:g.90815520C=	NCBI36
NG_033118.1:g.143422G=
NG_033118.2:g.143422G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.4700-117G= MANE Select	ENSP00000374507.6:n.4700-117G=
ENST00000331194.8:c.272-117G=	ENSP00000330332.8:n.272-117G=
ENST00000334448.5:n.512-117G=
ENST00000389857.10:c.4700-117G=	ENSP00000374507.6:n.4700-117G=
ENST00000556726.5:c.928-117G=
ENST00000557455.1:n.555G=
NM_001080414.3:c.4700-117G=	NP_001073883.2:n.4700-117G=
XM_011536796.1:c.4592-117G=	XP_011535098.1:n.4592-117G=
XR_429316.2:n.4975-117G=
XR_943459.1:n.5466G=
XM_011536796.2:c.4592-117G=	XP_011535098.1:n.4592-117G=
XM_017021335.2:c.*457G=	XP_016876824.1:n.*457G=
XM_017021336.1:c.1781-117G=	XP_016876825.1:n.1781-117G=
XR_429316.4:n.4973-117G=
NM_001080414.4:c.4700-117G= MANE Select	NP_001073883.2:n.4700-117G=