Canonical Allele Identifier: CA2802580902

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272347_91272348insCGT , CM000676.2:g.91272347_91272348insCGT	GRCh38
NC_000014.8:g.91738691_91738692insCGT , CM000676.1:g.91738691_91738692insCGT	GRCh37
NC_000014.7:g.90808444_90808445insCGT	NCBI36
NG_033118.1:g.150497_150498insACG
NG_033118.2:g.150497_150498insACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.*277_*278insACG MANE Select	ENSP00000374507.6:n.*277_*278insACG
ENST00000331194.8:c.*277_*278insACG	ENSP00000330332.8:n.*277_*278insACG
ENST00000389857.10:c.*277_*278insACG	ENSP00000374507.6:n.*277_*278insACG
ENST00000556726.5:c.2592_2593insACG
NM_001080414.3:c.*277_*278insACG	NP_001073883.2:n.*277_*278insACG
XM_011536796.1:c.*277_*278insACG	XP_011535098.1:n.*277_*278insACG
XM_011536796.2:c.*277_*278insACG	XP_011535098.1:n.*277_*278insACG
XM_017021336.1:c.*277_*278insACG	XP_016876825.1:n.*277_*278insACG
NM_001080414.4:c.*277_*278insACG MANE Select	NP_001073883.2:n.*277_*278insACG