Canonical Allele Identifier: CA2154899766

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272484_91272488delinsGAACA , CM000676.2:g.91272484_91272488delinsGAACA	GRCh38
NC_000014.8:g.91738828_91738832delinsGAACA , CM000676.1:g.91738828_91738832delinsGAACA	GRCh37
NC_000014.7:g.90808581_90808585delinsGAACA	NCBI36
NG_033118.1:g.150357_150361delinsTGTTC
NG_033118.2:g.150357_150361delinsTGTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.*137_*141delinsTGTTC MANE Select	ENSP00000374507.6:n.*137_*141delinsTGTTC
ENST00000331194.8:c.*137_*141delinsTGTTC	ENSP00000330332.8:n.*137_*141delinsTGTTC
ENST00000389857.10:c.*137_*141delinsTGTTC	ENSP00000374507.6:n.*137_*141delinsTGTTC
ENST00000556726.5:c.2452_2456delinsTGTTC
NM_001080414.3:c.*137_*141delinsTGTTC	NP_001073883.2:n.*137_*141delinsTGTTC
XM_011536796.1:c.*137_*141delinsTGTTC	XP_011535098.1:n.*137_*141delinsTGTTC
XM_011536796.2:c.*137_*141delinsTGTTC	XP_011535098.1:n.*137_*141delinsTGTTC
XM_017021336.1:c.*137_*141delinsTGTTC	XP_016876825.1:n.*137_*141delinsTGTTC
NM_001080414.4:c.*137_*141delinsTGTTC MANE Select	NP_001073883.2:n.*137_*141delinsTGTTC