Canonical Allele Identifier: CA2997496379

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91338149dup , CM000676.2:g.91338149dup	GRCh38
NC_000014.8:g.91804493dup , CM000676.1:g.91804493dup	GRCh37
NC_000014.7:g.90874246dup	NCBI36
NG_033118.1:g.84697dup
NG_033118.2:g.84697dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.907dup MANE Select	ENSP00000374507.6:p.Ala303GlyfsTer?
ENST00000389857.10:c.907dup	ENSP00000374507.6:p.Ala303GlyfsTer?
ENST00000554051.1:n.384dup
NM_001080414.3:c.907dup	NP_001073883.2:p.Ala303GlyfsTer?
XM_005267691.3:c.907dup	XP_005267748.1:p.Ala303GlyfsTer?
XM_011536796.1:c.799dup	XP_011535098.1:p.Ala267GlyfsTer?
XR_429316.2:n.1035dup
XR_943459.1:n.1035dup
XM_005267691.5:c.907dup	XP_005267748.1:p.Ala303GlyfsTer?
XM_011536796.2:c.799dup	XP_011535098.1:p.Ala267GlyfsTer?
XM_017021335.2:c.907dup	XP_016876824.1:p.Ala303GlyfsTer?
XM_017021337.2:c.907dup	XP_016876826.1:p.Ala303GlyfsTer?
XR_429316.4:n.1033dup
NM_001080414.4:c.907dup MANE Select	NP_001073883.2:p.Ala303GlyfsTer?