Canonical Allele Identifier: CA2154901188

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91305744_91305746delinsGGT , CM000676.2:g.91305744_91305746delinsGGT	GRCh38
NC_000014.8:g.91772088_91772090delinsGGT , CM000676.1:g.91772088_91772090delinsGGT	GRCh37
NC_000014.7:g.90841841_90841843delinsGGT	NCBI36
NG_033118.1:g.117099_117101delinsACC
NG_033118.2:g.117099_117101delinsACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.3357+19_3357+21delinsACC MANE Select	ENSP00000374507.6:n.3357+19_3357+21delinsACC
ENST00000389857.10:c.3357+19_3357+21delinsACC	ENSP00000374507.6:n.3357+19_3357+21delinsACC
NM_001080414.3:c.3357+19_3357+21delinsACC	NP_001073883.2:n.3357+19_3357+21delinsACC
XM_005267691.3:c.3357+19_3357+21delinsACC	XP_005267748.1:n.3357+19_3357+21delinsACC
XM_011536796.1:c.3249+19_3249+21delinsACC	XP_011535098.1:n.3249+19_3249+21delinsACC
XR_429316.2:n.3485+19_3485+21delinsACC
XR_943459.1:n.3485+19_3485+21delinsACC
XM_005267691.5:c.3357+19_3357+21delinsACC	XP_005267748.1:n.3357+19_3357+21delinsACC
XM_011536796.2:c.3249+19_3249+21delinsACC	XP_011535098.1:n.3249+19_3249+21delinsACC
XM_017021335.2:c.3357+19_3357+21delinsACC	XP_016876824.1:n.3357+19_3357+21delinsACC
XM_017021336.1:c.438+19_438+21delinsACC	XP_016876825.1:n.438+19_438+21delinsACC
XR_429316.4:n.3483+19_3483+21delinsACC
NM_001080414.4:c.3357+19_3357+21delinsACC MANE Select	NP_001073883.2:n.3357+19_3357+21delinsACC