Canonical Allele Identifier: CA2154899749

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272464_91272466delinsGCA , CM000676.2:g.91272464_91272466delinsGCA	GRCh38
NC_000014.8:g.91738808_91738810delinsGCA , CM000676.1:g.91738808_91738810delinsGCA	GRCh37
NC_000014.7:g.90808561_90808563delinsGCA	NCBI36
NG_033118.1:g.150379_150381delinsTGC
NG_033118.2:g.150379_150381delinsTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.*159_*161delinsTGC MANE Select	ENSP00000374507.6:n.*159_*161delinsTGC
ENST00000331194.8:c.*159_*161delinsTGC	ENSP00000330332.8:n.*159_*161delinsTGC
ENST00000389857.10:c.*159_*161delinsTGC	ENSP00000374507.6:n.*159_*161delinsTGC
ENST00000556726.5:c.2474_2476delinsTGC
NM_001080414.3:c.*159_*161delinsTGC	NP_001073883.2:n.*159_*161delinsTGC
XM_011536796.1:c.*159_*161delinsTGC	XP_011535098.1:n.*159_*161delinsTGC
XM_011536796.2:c.*159_*161delinsTGC	XP_011535098.1:n.*159_*161delinsTGC
XM_017021336.1:c.*159_*161delinsTGC	XP_016876825.1:n.*159_*161delinsTGC
NM_001080414.4:c.*159_*161delinsTGC MANE Select	NP_001073883.2:n.*159_*161delinsTGC