Canonical Allele Identifier: CA2154878536

Gene: CCDC88C

Linked Data

• dbSNP Id: rs1891919863

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91313251dup , CM000676.2:g.91313251dup	GRCh38
NC_000014.8:g.91779595dup , CM000676.1:g.91779595dup	GRCh37
NC_000014.7:g.90849348dup	NCBI36
NG_033118.1:g.109595dup
NG_033118.2:g.109595dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.2566dup MANE Select	ENSP00000374507.6:p.Asp856GlyfsTer3
ENST00000389857.10:c.2566dup	ENSP00000374507.6:p.Asp856GlyfsTer3
NM_001080414.3:c.2566dup	NP_001073883.2:p.Asp856GlyfsTer3
XM_005267691.3:c.2566dup	XP_005267748.1:p.Asp856GlyfsTer3
XM_011536796.1:c.2458dup	XP_011535098.1:p.Asp820GlyfsTer3
XR_429316.2:n.2694dup
XR_943459.1:n.2694dup
XM_005267691.5:c.2566dup	XP_005267748.1:p.Asp856GlyfsTer3
XM_011536796.2:c.2458dup	XP_011535098.1:p.Asp820GlyfsTer3
XM_017021335.2:c.2566dup	XP_016876824.1:p.Asp856GlyfsTer3
XM_017021337.2:c.2566dup	XP_016876826.1:p.Asp856GlyfsTer3
XR_429316.4:n.2692dup
NM_001080414.4:c.2566dup MANE Select	NP_001073883.2:p.Asp856GlyfsTer3