Canonical Allele Identifier: CA2154912741

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91338278_91338279delinsTG , CM000676.2:g.91338278_91338279delinsTG	GRCh38
NC_000014.8:g.91804622_91804623delinsTG , CM000676.1:g.91804622_91804623delinsTG	GRCh37
NC_000014.7:g.90874375_90874376delinsTG	NCBI36
NG_033118.1:g.84566_84567delinsCA
NG_033118.2:g.84566_84567delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.892-116_892-115delinsCA MANE Select	ENSP00000374507.6:n.892-116_892-115delinsCA
ENST00000389857.10:c.892-116_892-115delinsCA	ENSP00000374507.6:n.892-116_892-115delinsCA
ENST00000554051.1:n.369-116_369-115delinsCA
NM_001080414.3:c.892-116_892-115delinsCA	NP_001073883.2:n.892-116_892-115delinsCA
XM_005267691.3:c.892-116_892-115delinsCA	XP_005267748.1:n.892-116_892-115delinsCA
XM_011536796.1:c.784-116_784-115delinsCA	XP_011535098.1:n.784-116_784-115delinsCA
XR_429316.2:n.1020-116_1020-115delinsCA
XR_943459.1:n.1020-116_1020-115delinsCA
XM_005267691.5:c.892-116_892-115delinsCA	XP_005267748.1:n.892-116_892-115delinsCA
XM_011536796.2:c.784-116_784-115delinsCA	XP_011535098.1:n.784-116_784-115delinsCA
XM_017021335.2:c.892-116_892-115delinsCA	XP_016876824.1:n.892-116_892-115delinsCA
XM_017021337.2:c.892-116_892-115delinsCA	XP_016876826.1:n.892-116_892-115delinsCA
XR_429316.4:n.1018-116_1018-115delinsCA
NM_001080414.4:c.892-116_892-115delinsCA MANE Select	NP_001073883.2:n.892-116_892-115delinsCA