Canonical Allele Identifier: CA2154912596

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91337984C= , CM000676.2:g.91337984C=	GRCh38
NC_000014.8:g.91804328C= , CM000676.1:g.91804328C=	GRCh37
NC_000014.7:g.90874081C=	NCBI36
NG_033118.1:g.84861G=
NG_033118.2:g.84861G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.1050+21G= MANE Select	ENSP00000374507.6:n.1050+21G=
ENST00000389857.10:c.1050+21G=	ENSP00000374507.6:n.1050+21G=
NM_001080414.3:c.1050+21G=	NP_001073883.2:n.1050+21G=
XM_005267691.3:c.1050+21G=	XP_005267748.1:n.1050+21G=
XM_011536796.1:c.942+21G=	XP_011535098.1:n.942+21G=
XR_429316.2:n.1178+21G=
XR_943459.1:n.1178+21G=
XM_005267691.5:c.1050+21G=	XP_005267748.1:n.1050+21G=
XM_011536796.2:c.942+21G=	XP_011535098.1:n.942+21G=
XM_017021335.2:c.1050+21G=	XP_016876824.1:n.1050+21G=
XM_017021337.2:c.1050+21G=	XP_016876826.1:n.1050+21G=
XR_429316.4:n.1176+21G=
NM_001080414.4:c.1050+21G= MANE Select	NP_001073883.2:n.1050+21G=