Canonical Allele Identifier: CA2154899680

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272408G= , CM000676.2:g.91272408G=	GRCh38
NC_000014.8:g.91738752G= , CM000676.1:g.91738752G=	GRCh37
NC_000014.7:g.90808505G=	NCBI36
NG_033118.1:g.150437C=
NG_033118.2:g.150437C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.*217C= MANE Select	ENSP00000374507.6:n.*217C=
ENST00000331194.8:c.*217C=	ENSP00000330332.8:n.*217C=
ENST00000389857.10:c.*217C=	ENSP00000374507.6:n.*217C=
ENST00000556726.5:c.2532C=
NM_001080414.3:c.*217C=	NP_001073883.2:n.*217C=
XM_011536796.1:c.*217C=	XP_011535098.1:n.*217C=
XM_011536796.2:c.*217C=	XP_011535098.1:n.*217C=
XM_017021336.1:c.*217C=	XP_016876825.1:n.*217C=
NM_001080414.4:c.*217C= MANE Select	NP_001073883.2:n.*217C=