Canonical Allele Identifier: CA2154878195

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91312959_91312960delinsAG , CM000676.2:g.91312959_91312960delinsAG	GRCh38
NC_000014.8:g.91779303_91779304delinsAG , CM000676.1:g.91779303_91779304delinsAG	GRCh37
NC_000014.7:g.90849056_90849057delinsAG	NCBI36
NG_033118.1:g.109885_109886delinsCT
NG_033118.2:g.109885_109886delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.2736+120_2736+121delinsCT MANE Select	ENSP00000374507.6:n.2736+120_2736+121delinsCT
ENST00000389857.10:c.2736+120_2736+121delinsCT	ENSP00000374507.6:n.2736+120_2736+121delinsCT
NM_001080414.3:c.2736+120_2736+121delinsCT	NP_001073883.2:n.2736+120_2736+121delinsCT
XM_005267691.3:c.2736+120_2736+121delinsCT	XP_005267748.1:n.2736+120_2736+121delinsCT
XM_011536796.1:c.2628+120_2628+121delinsCT	XP_011535098.1:n.2628+120_2628+121delinsCT
XR_429316.2:n.2864+120_2864+121delinsCT
XR_943459.1:n.2864+120_2864+121delinsCT
XM_005267691.5:c.2736+120_2736+121delinsCT	XP_005267748.1:n.2736+120_2736+121delinsCT
XM_011536796.2:c.2628+120_2628+121delinsCT	XP_011535098.1:n.2628+120_2628+121delinsCT
XM_017021335.2:c.2736+120_2736+121delinsCT	XP_016876824.1:n.2736+120_2736+121delinsCT
XM_017021336.1:c.-56+120_-56+121delinsCT	XP_016876825.1:n.-56+120_-56+121delinsCT
XM_017021337.2:c.2736+120_2736+121delinsCT	XP_016876826.1:n.2736+120_2736+121delinsCT
XR_429316.4:n.2862+120_2862+121delinsCT
NM_001080414.4:c.2736+120_2736+121delinsCT MANE Select	NP_001073883.2:n.2736+120_2736+121delinsCT