Canonical Allele Identifier: CA2154878511

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91313241_91313282delinsTGCTATCGTCCAAGACTGCATCCTTGAGCTCCACCTGCTGCC , CM000676.2:g.91313241_91313282delinsTGCTATCGTCCAAGACTGCATCCTTGAGCTCCACCTGCTGCC	GRCh38
NC_000014.8:g.91779585_91779626delinsTGCTATCGTCCAAGACTGCATCCTTGAGCTCCACCTGCTGCC , CM000676.1:g.91779585_91779626delinsTGCTATCGTCCAAGACTGCATCCTTGAGCTCCACCTGCTGCC	GRCh37
NC_000014.7:g.90849338_90849379delinsTGCTATCGTCCAAGACTGCATCCTTGAGCTCCACCTGCTGCC	NCBI36
NG_033118.1:g.109563_109604delinsGGCAGCAGGTGGAGCTCAAGGATGCAGTCTTGGACGATAGCA
NG_033118.2:g.109563_109604delinsGGCAGCAGGTGGAGCTCAAGGATGCAGTCTTGGACGATAGCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.2534_2575delinsGGCAGCAGGTGGAGCTCAAGGATGCAGTCTTGGACGATAGCA MANE Select	ENSP00000374507.6:p.Trp845=
ENST00000389857.10:c.2534_2575delinsGGCAGCAGGTGGAGCTCAAGGATGCAGTCTTGGACGATAGCA	ENSP00000374507.6:p.Trp845=
NM_001080414.3:c.2534_2575delinsGGCAGCAGGTGGAGCTCAAGGATGCAGTCTTGGACGATAGCA	NP_001073883.2:p.Trp845=
XM_005267691.3:c.2534_2575delinsGGCAGCAGGTGGAGCTCAAGGATGCAGTCTTGGACGATAGCA	XP_005267748.1:p.Trp845=
XM_011536796.1:c.2426_2467delinsGGCAGCAGGTGGAGCTCAAGGATGCAGTCTTGGACGATAGCA	XP_011535098.1:p.Trp809=
XR_429316.2:n.2662_2703delinsGGCAGCAGGTGGAGCTCAAGGATGCAGTCTTGGACGATAGCA
XR_943459.1:n.2662_2703delinsGGCAGCAGGTGGAGCTCAAGGATGCAGTCTTGGACGATAGCA
XM_005267691.5:c.2534_2575delinsGGCAGCAGGTGGAGCTCAAGGATGCAGTCTTGGACGATAGCA	XP_005267748.1:p.Trp845=
XM_011536796.2:c.2426_2467delinsGGCAGCAGGTGGAGCTCAAGGATGCAGTCTTGGACGATAGCA	XP_011535098.1:p.Trp809=
XM_017021335.2:c.2534_2575delinsGGCAGCAGGTGGAGCTCAAGGATGCAGTCTTGGACGATAGCA	XP_016876824.1:p.Trp845=
XM_017021337.2:c.2534_2575delinsGGCAGCAGGTGGAGCTCAAGGATGCAGTCTTGGACGATAGCA	XP_016876826.1:p.Trp845=
XR_429316.4:n.2660_2701delinsGGCAGCAGGTGGAGCTCAAGGATGCAGTCTTGGACGATAGCA
NM_001080414.4:c.2534_2575delinsGGCAGCAGGTGGAGCTCAAGGATGCAGTCTTGGACGATAGCA MANE Select	NP_001073883.2:p.Trp845=