Canonical Allele Identifier: CA2517526059

Gene: CCDC88C

Linked Data

• gnomAD v4: 14-91338225-GCCAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91338226_91338229del , CM000676.2:g.91338226_91338229del	GRCh38
NC_000014.8:g.91804570_91804573del , CM000676.1:g.91804570_91804573del	GRCh37
NC_000014.7:g.90874323_90874326del	NCBI36
NG_033118.1:g.84616_84619del
NG_033118.2:g.84616_84619del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.892-66_892-63del MANE Select	ENSP00000374507.6:n.892-66_892-63del
ENST00000389857.10:c.892-66_892-63del	ENSP00000374507.6:n.892-66_892-63del
ENST00000554051.1:n.369-66_369-63del
NM_001080414.3:c.892-66_892-63del	NP_001073883.2:n.892-66_892-63del
XM_005267691.3:c.892-66_892-63del	XP_005267748.1:n.892-66_892-63del
XM_011536796.1:c.784-66_784-63del	XP_011535098.1:n.784-66_784-63del
XR_429316.2:n.1020-66_1020-63del
XR_943459.1:n.1020-66_1020-63del
XM_005267691.5:c.892-66_892-63del	XP_005267748.1:n.892-66_892-63del
XM_011536796.2:c.784-66_784-63del	XP_011535098.1:n.784-66_784-63del
XM_017021335.2:c.892-66_892-63del	XP_016876824.1:n.892-66_892-63del
XM_017021337.2:c.892-66_892-63del	XP_016876826.1:n.892-66_892-63del
XR_429316.4:n.1018-66_1018-63del
NM_001080414.4:c.892-66_892-63del MANE Select	NP_001073883.2:n.892-66_892-63del