Canonical Allele Identifier: CA2626130641

Gene: CCDC88C

Linked Data

• gnomAD v4: 14-91313307-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91313308del , CM000676.2:g.91313308del	GRCh38
NC_000014.8:g.91779652del , CM000676.1:g.91779652del	GRCh37
NC_000014.7:g.90849405del	NCBI36
NG_033118.1:g.109537del
NG_033118.2:g.109537del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.2508del MANE Select	ENSP00000374507.6:p.Leu837TrpfsTer?
ENST00000389857.10:c.2508del	ENSP00000374507.6:p.Leu837TrpfsTer?
NM_001080414.3:c.2508del	NP_001073883.2:p.Leu837TrpfsTer?
XM_005267691.3:c.2508del	XP_005267748.1:p.Leu837TrpfsTer?
XM_011536796.1:c.2400del	XP_011535098.1:p.Leu801TrpfsTer?
XR_429316.2:n.2636del
XR_943459.1:n.2636del
XM_005267691.5:c.2508del	XP_005267748.1:p.Leu837TrpfsTer?
XM_011536796.2:c.2400del	XP_011535098.1:p.Leu801TrpfsTer?
XM_017021335.2:c.2508del	XP_016876824.1:p.Leu837TrpfsTer?
XM_017021337.2:c.2508del	XP_016876826.1:p.Leu837TrpfsTer?
XR_429316.4:n.2634del
NM_001080414.4:c.2508del MANE Select	NP_001073883.2:p.Leu837TrpfsTer?