Canonical Allele Identifier: CA2154901046

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91305659_91305660delinsTG , CM000676.2:g.91305659_91305660delinsTG	GRCh38
NC_000014.8:g.91772003_91772004delinsTG , CM000676.1:g.91772003_91772004delinsTG	GRCh37
NC_000014.7:g.90841756_90841757delinsTG	NCBI36
NG_033118.1:g.117185_117186delinsCA
NG_033118.2:g.117185_117186delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.3357+105_3357+106delinsCA MANE Select	ENSP00000374507.6:n.3357+105_3357+106delinsCA
ENST00000389857.10:c.3357+105_3357+106delinsCA	ENSP00000374507.6:n.3357+105_3357+106delinsCA
NM_001080414.3:c.3357+105_3357+106delinsCA	NP_001073883.2:n.3357+105_3357+106delinsCA
XM_005267691.3:c.3357+105_3357+106delinsCA	XP_005267748.1:n.3357+105_3357+106delinsCA
XM_011536796.1:c.3249+105_3249+106delinsCA	XP_011535098.1:n.3249+105_3249+106delinsCA
XR_429316.2:n.3485+105_3485+106delinsCA
XR_943459.1:n.3485+105_3485+106delinsCA
XM_005267691.5:c.3357+105_3357+106delinsCA	XP_005267748.1:n.3357+105_3357+106delinsCA
XM_011536796.2:c.3249+105_3249+106delinsCA	XP_011535098.1:n.3249+105_3249+106delinsCA
XM_017021335.2:c.3357+105_3357+106delinsCA	XP_016876824.1:n.3357+105_3357+106delinsCA
XM_017021336.1:c.438+105_438+106delinsCA	XP_016876825.1:n.438+105_438+106delinsCA
XR_429316.4:n.3483+105_3483+106delinsCA
NM_001080414.4:c.3357+105_3357+106delinsCA MANE Select	NP_001073883.2:n.3357+105_3357+106delinsCA