Canonical Allele Identifier: CA2154901667

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91306098_91306099delinsAT , CM000676.2:g.91306098_91306099delinsAT	GRCh38
NC_000014.8:g.91772442_91772443delinsAT , CM000676.1:g.91772442_91772443delinsAT	GRCh37
NC_000014.7:g.90842195_90842196delinsAT	NCBI36
NG_033118.1:g.116746_116747delinsAT
NG_033118.2:g.116746_116747delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.3196-173_3196-172delinsAT MANE Select	ENSP00000374507.6:n.3196-173_3196-172delinsAT
ENST00000389857.10:c.3196-173_3196-172delinsAT	ENSP00000374507.6:n.3196-173_3196-172delinsAT
NM_001080414.3:c.3196-173_3196-172delinsAT	NP_001073883.2:n.3196-173_3196-172delinsAT
XM_005267691.3:c.3196-173_3196-172delinsAT	XP_005267748.1:n.3196-173_3196-172delinsAT
XM_011536796.1:c.3088-173_3088-172delinsAT	XP_011535098.1:n.3088-173_3088-172delinsAT
XR_429316.2:n.3324-173_3324-172delinsAT
XR_943459.1:n.3324-173_3324-172delinsAT
XM_005267691.5:c.3196-173_3196-172delinsAT	XP_005267748.1:n.3196-173_3196-172delinsAT
XM_011536796.2:c.3088-173_3088-172delinsAT	XP_011535098.1:n.3088-173_3088-172delinsAT
XM_017021335.2:c.3196-173_3196-172delinsAT	XP_016876824.1:n.3196-173_3196-172delinsAT
XM_017021336.1:c.277-173_277-172delinsAT	XP_016876825.1:n.277-173_277-172delinsAT
XR_429316.4:n.3322-173_3322-172delinsAT
NM_001080414.4:c.3196-173_3196-172delinsAT MANE Select	NP_001073883.2:n.3196-173_3196-172delinsAT