Canonical Allele Identifier: CA2154899613

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272365_91272366delinsTG , CM000676.2:g.91272365_91272366delinsTG	GRCh38
NC_000014.8:g.91738709_91738710delinsTG , CM000676.1:g.91738709_91738710delinsTG	GRCh37
NC_000014.7:g.90808462_90808463delinsTG	NCBI36
NG_033118.1:g.150479_150480delinsCA
NG_033118.2:g.150479_150480delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.*259_*260delinsCA MANE Select	ENSP00000374507.6:n.*259_*260delinsCA
ENST00000331194.8:c.*259_*260delinsCA	ENSP00000330332.8:n.*259_*260delinsCA
ENST00000389857.10:c.*259_*260delinsCA	ENSP00000374507.6:n.*259_*260delinsCA
ENST00000556726.5:c.2574_2575delinsCA
NM_001080414.3:c.*259_*260delinsCA	NP_001073883.2:n.*259_*260delinsCA
XM_011536796.1:c.*259_*260delinsCA	XP_011535098.1:n.*259_*260delinsCA
XM_011536796.2:c.*259_*260delinsCA	XP_011535098.1:n.*259_*260delinsCA
XM_017021336.1:c.*259_*260delinsCA	XP_016876825.1:n.*259_*260delinsCA
NM_001080414.4:c.*259_*260delinsCA MANE Select	NP_001073883.2:n.*259_*260delinsCA