Canonical Allele Identifier: CA2802580903

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272352_91272353insTAAAAAAAGAG , CM000676.2:g.91272352_91272353insTAAAAAAAGAG	GRCh38
NC_000014.8:g.91738696_91738697insTAAAAAAAGAG , CM000676.1:g.91738696_91738697insTAAAAAAAGAG	GRCh37
NC_000014.7:g.90808449_90808450insTAAAAAAAGAG	NCBI36
NG_033118.1:g.150492_150493insCTCTTTTTTTA
NG_033118.2:g.150492_150493insCTCTTTTTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.*272_*273insCTCTTTTTTTA MANE Select	ENSP00000374507.6:n.*272_*273insCTCTTTTTTTA
ENST00000331194.8:c.*272_*273insCTCTTTTTTTA	ENSP00000330332.8:n.*272_*273insCTCTTTTTTTA
ENST00000389857.10:c.*272_*273insCTCTTTTTTTA	ENSP00000374507.6:n.*272_*273insCTCTTTTTTTA
ENST00000556726.5:c.2587_2588insCTCTTTTTTTA
NM_001080414.3:c.*272_*273insCTCTTTTTTTA	NP_001073883.2:n.*272_*273insCTCTTTTTTTA
XM_011536796.1:c.*272_*273insCTCTTTTTTTA	XP_011535098.1:n.*272_*273insCTCTTTTTTTA
XM_011536796.2:c.*272_*273insCTCTTTTTTTA	XP_011535098.1:n.*272_*273insCTCTTTTTTTA
XM_017021336.1:c.*272_*273insCTCTTTTTTTA	XP_016876825.1:n.*272_*273insCTCTTTTTTTA
NM_001080414.4:c.*272_*273insCTCTTTTTTTA MANE Select	NP_001073883.2:n.*272_*273insCTCTTTTTTTA