Canonical Allele Identifier: CA2626131023

Gene: CCDC88C

Linked Data

• gnomAD v4: 14-91337989-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91337990dup , CM000676.2:g.91337990dup	GRCh38
NC_000014.8:g.91804334dup , CM000676.1:g.91804334dup	GRCh37
NC_000014.7:g.90874087dup	NCBI36
NG_033118.1:g.84855dup
NG_033118.2:g.84855dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.1050+15dup MANE Select	ENSP00000374507.6:n.1050+15dup
ENST00000389857.10:c.1050+15dup	ENSP00000374507.6:n.1050+15dup
NM_001080414.3:c.1050+15dup	NP_001073883.2:n.1050+15dup
XM_005267691.3:c.1050+15dup	XP_005267748.1:n.1050+15dup
XM_011536796.1:c.942+15dup	XP_011535098.1:n.942+15dup
XR_429316.2:n.1178+15dup
XR_943459.1:n.1178+15dup
XM_005267691.5:c.1050+15dup	XP_005267748.1:n.1050+15dup
XM_011536796.2:c.942+15dup	XP_011535098.1:n.942+15dup
XM_017021335.2:c.1050+15dup	XP_016876824.1:n.1050+15dup
XM_017021337.2:c.1050+15dup	XP_016876826.1:n.1050+15dup
XR_429316.4:n.1176+15dup
NM_001080414.4:c.1050+15dup MANE Select	NP_001073883.2:n.1050+15dup