Canonical Allele Identifier: CA709883754

Gene: CCDC88C

Linked Data

• dbSNP Id: rs1343578731
• MyVariant Identifiers: chr14:g.91804568_91804570del (hg19) ; chr14:g.91338224_91338226del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91338224_91338226del , CM000676.2:g.91338224_91338226del	GRCh38
NC_000014.8:g.91804568_91804570del , CM000676.1:g.91804568_91804570del	GRCh37
NC_000014.7:g.90874321_90874323del	NCBI36
NG_033118.1:g.84619_84621del
NG_033118.2:g.84619_84621del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.892-63_892-61del MANE Select	ENSP00000374507.6:n.892-63_892-61del
ENST00000389857.10:c.892-63_892-61del	ENSP00000374507.6:n.892-63_892-61del
ENST00000554051.1:n.369-63_369-61del
NM_001080414.3:c.892-63_892-61del	NP_001073883.2:n.892-63_892-61del
XM_005267691.3:c.892-63_892-61del	XP_005267748.1:n.892-63_892-61del
XM_011536796.1:c.784-63_784-61del	XP_011535098.1:n.784-63_784-61del
XR_429316.2:n.1020-63_1020-61del
XR_943459.1:n.1020-63_1020-61del
XM_005267691.5:c.892-63_892-61del	XP_005267748.1:n.892-63_892-61del
XM_011536796.2:c.784-63_784-61del	XP_011535098.1:n.784-63_784-61del
XM_017021335.2:c.892-63_892-61del	XP_016876824.1:n.892-63_892-61del
XM_017021337.2:c.892-63_892-61del	XP_016876826.1:n.892-63_892-61del
XR_429316.4:n.1018-63_1018-61del
NM_001080414.4:c.892-63_892-61del MANE Select	NP_001073883.2:n.892-63_892-61del