Canonical Allele Identifier: CA2154899688

Gene: CCDC88C

Linked Data

• dbSNP Id: rs1889772944

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272420_91272421del , CM000676.2:g.91272420_91272421del	GRCh38
NC_000014.8:g.91738764_91738765del , CM000676.1:g.91738764_91738765del	GRCh37
NC_000014.7:g.90808517_90808518del	NCBI36
NG_033118.1:g.150425_150426del
NG_033118.2:g.150425_150426del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.*205_*206del MANE Select	ENSP00000374507.6:n.*205_*206del
ENST00000331194.8:c.*205_*206del	ENSP00000330332.8:n.*205_*206del
ENST00000389857.10:c.*205_*206del	ENSP00000374507.6:n.*205_*206del
ENST00000556726.5:c.2520_2521del
NM_001080414.3:c.*205_*206del	NP_001073883.2:n.*205_*206del
XM_011536796.1:c.*205_*206del	XP_011535098.1:n.*205_*206del
XM_011536796.2:c.*205_*206del	XP_011535098.1:n.*205_*206del
XM_017021336.1:c.*205_*206del	XP_016876825.1:n.*205_*206del
NM_001080414.4:c.*205_*206del MANE Select	NP_001073883.2:n.*205_*206del