Canonical Allele Identifier: CA2154878356

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91313147_91313186delinsTCCAGCTCCTTCAGCTTGCCGGCTGCGTCCCTGCAGCGGG , CM000676.2:g.91313147_91313186delinsTCCAGCTCCTTCAGCTTGCCGGCTGCGTCCCTGCAGCGGG	GRCh38
NC_000014.8:g.91779491_91779530delinsTCCAGCTCCTTCAGCTTGCCGGCTGCGTCCCTGCAGCGGG , CM000676.1:g.91779491_91779530delinsTCCAGCTCCTTCAGCTTGCCGGCTGCGTCCCTGCAGCGGG	GRCh37
NC_000014.7:g.90849244_90849283delinsTCCAGCTCCTTCAGCTTGCCGGCTGCGTCCCTGCAGCGGG	NCBI36
NG_033118.1:g.109659_109698delinsCCCGCTGCAGGGACGCAGCCGGCAAGCTGAAGGAGCTGGA
NG_033118.2:g.109659_109698delinsCCCGCTGCAGGGACGCAGCCGGCAAGCTGAAGGAGCTGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.2630_2669delinsCCCGCTGCAGGGACGCAGCCGGCAAGCTGAAGGAGCTGGA MANE Select	ENSP00000374507.6:p.Ala877=
ENST00000389857.10:c.2630_2669delinsCCCGCTGCAGGGACGCAGCCGGCAAGCTGAAGGAGCTGGA	ENSP00000374507.6:p.Ala877=
NM_001080414.3:c.2630_2669delinsCCCGCTGCAGGGACGCAGCCGGCAAGCTGAAGGAGCTGGA	NP_001073883.2:p.Ala877=
XM_005267691.3:c.2630_2669delinsCCCGCTGCAGGGACGCAGCCGGCAAGCTGAAGGAGCTGGA	XP_005267748.1:p.Ala877=
XM_011536796.1:c.2522_2561delinsCCCGCTGCAGGGACGCAGCCGGCAAGCTGAAGGAGCTGGA	XP_011535098.1:p.Ala841=
XR_429316.2:n.2758_2797delinsCCCGCTGCAGGGACGCAGCCGGCAAGCTGAAGGAGCTGGA
XR_943459.1:n.2758_2797delinsCCCGCTGCAGGGACGCAGCCGGCAAGCTGAAGGAGCTGGA
XM_005267691.5:c.2630_2669delinsCCCGCTGCAGGGACGCAGCCGGCAAGCTGAAGGAGCTGGA	XP_005267748.1:p.Ala877=
XM_011536796.2:c.2522_2561delinsCCCGCTGCAGGGACGCAGCCGGCAAGCTGAAGGAGCTGGA	XP_011535098.1:p.Ala841=
XM_017021335.2:c.2630_2669delinsCCCGCTGCAGGGACGCAGCCGGCAAGCTGAAGGAGCTGGA	XP_016876824.1:p.Ala877=
XM_017021337.2:c.2630_2669delinsCCCGCTGCAGGGACGCAGCCGGCAAGCTGAAGGAGCTGGA	XP_016876826.1:p.Ala877=
XR_429316.4:n.2756_2795delinsCCCGCTGCAGGGACGCAGCCGGCAAGCTGAAGGAGCTGGA
NM_001080414.4:c.2630_2669delinsCCCGCTGCAGGGACGCAGCCGGCAAGCTGAAGGAGCTGGA MANE Select	NP_001073883.2:p.Ala877=