Canonical Allele Identifier: CA2154912692

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91338176_91338177delinsCA , CM000676.2:g.91338176_91338177delinsCA	GRCh38
NC_000014.8:g.91804520_91804521delinsCA , CM000676.1:g.91804520_91804521delinsCA	GRCh37
NC_000014.7:g.90874273_90874274delinsCA	NCBI36
NG_033118.1:g.84668_84669delinsTG
NG_033118.2:g.84668_84669delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.892-14_892-13delinsTG MANE Select	ENSP00000374507.6:n.892-14_892-13delinsTG...
ENST00000389857.10:c.892-14_892-13delinsTG	ENSP00000374507.6:n.892-14_892-13delinsTG...
ENST00000554051.1:n.369-14_369-13delinsTG
NM_001080414.3:c.892-14_892-13delinsTG	NP_001073883.2:n.892-14_892-13delinsTG
XM_005267691.3:c.892-14_892-13delinsTG	XP_005267748.1:n.892-14_892-13delinsTG
XM_011536796.1:c.784-14_784-13delinsTG	XP_011535098.1:n.784-14_784-13delinsTG
XR_429316.2:n.1020-14_1020-13delinsTG
XR_943459.1:n.1020-14_1020-13delinsTG
XM_005267691.5:c.892-14_892-13delinsTG	XP_005267748.1:n.892-14_892-13delinsTG
XM_011536796.2:c.784-14_784-13delinsTG	XP_011535098.1:n.784-14_784-13delinsTG
XM_017021335.2:c.892-14_892-13delinsTG	XP_016876824.1:n.892-14_892-13delinsTG
XM_017021337.2:c.892-14_892-13delinsTG	XP_016876826.1:n.892-14_892-13delinsTG
XR_429316.4:n.1018-14_1018-13delinsTG
NM_001080414.4:c.892-14_892-13delinsTG MANE Select	NP_001073883.2:n.892-14_892-13delinsTG