Canonical Allele Identifier: CA2154901439

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91305912_91305921delinsCTGCAGAGCT , CM000676.2:g.91305912_91305921delinsCTGCAGAGCT	GRCh38
NC_000014.8:g.91772256_91772265delinsCTGCAGAGCT , CM000676.1:g.91772256_91772265delinsCTGCAGAGCT	GRCh37
NC_000014.7:g.90842009_90842018delinsCTGCAGAGCT	NCBI36
NG_033118.1:g.116924_116933delinsAGCTCTGCAG
NG_033118.2:g.116924_116933delinsAGCTCTGCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.3201_3210delinsAGCTCTGCAG MANE Select	ENSP00000374507.6:p.Ala1067=
ENST00000389857.10:c.3201_3210delinsAGCTCTGCAG	ENSP00000374507.6:p.Ala1067=
NM_001080414.3:c.3201_3210delinsAGCTCTGCAG	NP_001073883.2:p.Ala1067=
XM_005267691.3:c.3201_3210delinsAGCTCTGCAG	XP_005267748.1:p.Ala1067=
XM_011536796.1:c.3093_3102delinsAGCTCTGCAG	XP_011535098.1:p.Ala1031=
XR_429316.2:n.3329_3338delinsAGCTCTGCAG
XR_943459.1:n.3329_3338delinsAGCTCTGCAG
XM_005267691.5:c.3201_3210delinsAGCTCTGCAG	XP_005267748.1:p.Ala1067=
XM_011536796.2:c.3093_3102delinsAGCTCTGCAG	XP_011535098.1:p.Ala1031=
XM_017021335.2:c.3201_3210delinsAGCTCTGCAG	XP_016876824.1:p.Ala1067=
XM_017021336.1:c.282_291delinsAGCTCTGCAG	XP_016876825.1:p.Ala94=
XR_429316.4:n.3327_3336delinsAGCTCTGCAG
NM_001080414.4:c.3201_3210delinsAGCTCTGCAG MANE Select	NP_001073883.2:p.Ala1067=