Canonical Allele Identifier: CA2154912621

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91338027T= , CM000676.2:g.91338027T=	GRCh38
NC_000014.8:g.91804371T= , CM000676.1:g.91804371T=	GRCh37
NC_000014.7:g.90874124T=	NCBI36
NG_033118.1:g.84818A=
NG_033118.2:g.84818A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.1028A= MANE Select	ENSP00000374507.6:p.Asp343=
ENST00000389857.10:c.1028A=	ENSP00000374507.6:p.Asp343=
NM_001080414.3:c.1028A=	NP_001073883.2:p.Asp343=
XM_005267691.3:c.1028A=	XP_005267748.1:p.Asp343=
XM_011536796.1:c.920A=	XP_011535098.1:p.Asp307=
XR_429316.2:n.1156A=
XR_943459.1:n.1156A=
XM_005267691.5:c.1028A=	XP_005267748.1:p.Asp343=
XM_011536796.2:c.920A=	XP_011535098.1:p.Asp307=
XM_017021335.2:c.1028A=	XP_016876824.1:p.Asp343=
XM_017021337.2:c.1028A=	XP_016876826.1:p.Asp343=
XR_429316.4:n.1154A=
NM_001080414.4:c.1028A= MANE Select	NP_001073883.2:p.Asp343=