Canonical Allele Identifier: CA2626126671

Gene: CCDC88C

Linked Data

• gnomAD v4: 14-91272340-G-GGA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272340_91272341insGA , CM000676.2:g.91272340_91272341insGA	GRCh38
NC_000014.8:g.91738684_91738685insGA , CM000676.1:g.91738684_91738685insGA	GRCh37
NC_000014.7:g.90808437_90808438insGA	NCBI36
NG_033118.1:g.150504_150505insTC
NG_033118.2:g.150504_150505insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.*284_*285insTC MANE Select	ENSP00000374507.6:n.*284_*285insTC
ENST00000331194.8:c.*284_*285insTC	ENSP00000330332.8:n.*284_*285insTC
ENST00000389857.10:c.*284_*285insTC	ENSP00000374507.6:n.*284_*285insTC
ENST00000556726.5:c.2599_2600insTC
NM_001080414.3:c.*284_*285insTC	NP_001073883.2:n.*284_*285insTC
XM_011536796.1:c.*284_*285insTC	XP_011535098.1:n.*284_*285insTC
XM_011536796.2:c.*284_*285insTC	XP_011535098.1:n.*284_*285insTC
XM_017021336.1:c.*284_*285insTC	XP_016876825.1:n.*284_*285insTC
NM_001080414.4:c.*284_*285insTC MANE Select	NP_001073883.2:n.*284_*285insTC