Canonical Allele Identifier: CA2154901008

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91305627_91305629delinsCTA , CM000676.2:g.91305627_91305629delinsCTA	GRCh38
NC_000014.8:g.91771971_91771973delinsCTA , CM000676.1:g.91771971_91771973delinsCTA	GRCh37
NC_000014.7:g.90841724_90841726delinsCTA	NCBI36
NG_033118.1:g.117216_117218delinsTAG
NG_033118.2:g.117216_117218delinsTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.3357+136_3357+138delinsTAG MANE Select	ENSP00000374507.6:n.3357+136_3357+138delinsTAG
ENST00000389857.10:c.3357+136_3357+138delinsTAG	ENSP00000374507.6:n.3357+136_3357+138delinsTAG
NM_001080414.3:c.3357+136_3357+138delinsTAG	NP_001073883.2:n.3357+136_3357+138delinsTAG
XM_005267691.3:c.3357+136_3357+138delinsTAG	XP_005267748.1:n.3357+136_3357+138delinsTAG
XM_011536796.1:c.3249+136_3249+138delinsTAG	XP_011535098.1:n.3249+136_3249+138delinsTAG
XR_429316.2:n.3485+136_3485+138delinsTAG
XR_943459.1:n.3485+136_3485+138delinsTAG
XM_005267691.5:c.3357+136_3357+138delinsTAG	XP_005267748.1:n.3357+136_3357+138delinsTAG
XM_011536796.2:c.3249+136_3249+138delinsTAG	XP_011535098.1:n.3249+136_3249+138delinsTAG
XM_017021335.2:c.3357+136_3357+138delinsTAG	XP_016876824.1:n.3357+136_3357+138delinsTAG
XM_017021336.1:c.438+136_438+138delinsTAG	XP_016876825.1:n.438+136_438+138delinsTAG
XR_429316.4:n.3483+136_3483+138delinsTAG
NM_001080414.4:c.3357+136_3357+138delinsTAG MANE Select	NP_001073883.2:n.3357+136_3357+138delinsTAG