Canonical Allele Identifier: CA2154900988

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91305610_91305612delinsCTG , CM000676.2:g.91305610_91305612delinsCTG	GRCh38
NC_000014.8:g.91771954_91771956delinsCTG , CM000676.1:g.91771954_91771956delinsCTG	GRCh37
NC_000014.7:g.90841707_90841709delinsCTG	NCBI36
NG_033118.1:g.117233_117235delinsCAG
NG_033118.2:g.117233_117235delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.3357+153_3357+155delinsCAG MANE Select	ENSP00000374507.6:n.3357+153_3357+155delinsCAG
ENST00000389857.10:c.3357+153_3357+155delinsCAG	ENSP00000374507.6:n.3357+153_3357+155delinsCAG
NM_001080414.3:c.3357+153_3357+155delinsCAG	NP_001073883.2:n.3357+153_3357+155delinsCAG
XM_005267691.3:c.3357+153_3357+155delinsCAG	XP_005267748.1:n.3357+153_3357+155delinsCAG
XM_011536796.1:c.3249+153_3249+155delinsCAG	XP_011535098.1:n.3249+153_3249+155delinsCAG
XR_429316.2:n.3485+153_3485+155delinsCAG
XR_943459.1:n.3485+153_3485+155delinsCAG
XM_005267691.5:c.3357+153_3357+155delinsCAG	XP_005267748.1:n.3357+153_3357+155delinsCAG
XM_011536796.2:c.3249+153_3249+155delinsCAG	XP_011535098.1:n.3249+153_3249+155delinsCAG
XM_017021335.2:c.3357+153_3357+155delinsCAG	XP_016876824.1:n.3357+153_3357+155delinsCAG
XM_017021336.1:c.438+153_438+155delinsCAG	XP_016876825.1:n.438+153_438+155delinsCAG
XR_429316.4:n.3483+153_3483+155delinsCAG
NM_001080414.4:c.3357+153_3357+155delinsCAG MANE Select	NP_001073883.2:n.3357+153_3357+155delinsCAG