Canonical Allele Identifier: CA2544013583

Gene: CCDC88C

Linked Data

• gnomAD v4: 14-91338231-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91338234del , CM000676.2:g.91338234del	GRCh38
NC_000014.8:g.91804578del , CM000676.1:g.91804578del	GRCh37
NC_000014.7:g.90874331del	NCBI36
NG_033118.1:g.84613del
NG_033118.2:g.84613del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.892-69del MANE Select	ENSP00000374507.6:n.892-69del
ENST00000389857.10:c.892-69del	ENSP00000374507.6:n.892-69del
ENST00000554051.1:n.369-69del
NM_001080414.3:c.892-69del	NP_001073883.2:n.892-69del
XM_005267691.3:c.892-69del	XP_005267748.1:n.892-69del
XM_011536796.1:c.784-69del	XP_011535098.1:n.784-69del
XR_429316.2:n.1020-69del
XR_943459.1:n.1020-69del
XM_005267691.5:c.892-69del	XP_005267748.1:n.892-69del
XM_011536796.2:c.784-69del	XP_011535098.1:n.784-69del
XM_017021335.2:c.892-69del	XP_016876824.1:n.892-69del
XM_017021337.2:c.892-69del	XP_016876826.1:n.892-69del
XR_429316.4:n.1018-69del
NM_001080414.4:c.892-69del MANE Select	NP_001073883.2:n.892-69del