Canonical Allele Identifier: CA2154899646

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272376_91272380delinsATTAT , CM000676.2:g.91272376_91272380delinsATTAT	GRCh38
NC_000014.8:g.91738720_91738724delinsATTAT , CM000676.1:g.91738720_91738724delinsATTAT	GRCh37
NC_000014.7:g.90808473_90808477delinsATTAT	NCBI36
NG_033118.1:g.150465_150469delinsATAAT
NG_033118.2:g.150465_150469delinsATAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.*245_*249delinsATAAT MANE Select	ENSP00000374507.6:n.*245_*249delinsATAAT
ENST00000331194.8:c.*245_*249delinsATAAT	ENSP00000330332.8:n.*245_*249delinsATAAT
ENST00000389857.10:c.*245_*249delinsATAAT	ENSP00000374507.6:n.*245_*249delinsATAAT
ENST00000556726.5:c.2560_2564delinsATAAT
NM_001080414.3:c.*245_*249delinsATAAT	NP_001073883.2:n.*245_*249delinsATAAT
XM_011536796.1:c.*245_*249delinsATAAT	XP_011535098.1:n.*245_*249delinsATAAT
XM_011536796.2:c.*245_*249delinsATAAT	XP_011535098.1:n.*245_*249delinsATAAT
XM_017021336.1:c.*245_*249delinsATAAT	XP_016876825.1:n.*245_*249delinsATAAT
NM_001080414.4:c.*245_*249delinsATAAT MANE Select	NP_001073883.2:n.*245_*249delinsATAAT