Canonical Allele Identifier: CA919477242

Gene: CCDC88C

Linked Data

• dbSNP Id: rs869299267

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272379_91272381dup , CM000676.2:g.91272379_91272381dup	GRCh38
NC_000014.8:g.91738723_91738725dup , CM000676.1:g.91738723_91738725dup	GRCh37
NC_000014.7:g.90808476_90808478dup	NCBI36
NG_033118.1:g.150467_150469dup
NG_033118.2:g.150467_150469dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.*247_*249dup MANE Select	ENSP00000374507.6:n.*247_*249dup
ENST00000331194.8:c.*247_*249dup	ENSP00000330332.8:n.*247_*249dup
ENST00000389857.10:c.*247_*249dup	ENSP00000374507.6:n.*247_*249dup
ENST00000556726.5:c.2562_2564dup
NM_001080414.3:c.*247_*249dup	NP_001073883.2:n.*247_*249dup
XM_011536796.1:c.*247_*249dup	XP_011535098.1:n.*247_*249dup
XM_011536796.2:c.*247_*249dup	XP_011535098.1:n.*247_*249dup
XM_017021336.1:c.*247_*249dup	XP_016876825.1:n.*247_*249dup
NM_001080414.4:c.*247_*249dup MANE Select	NP_001073883.2:n.*247_*249dup