Canonical Allele Identifier: CA2626123496

Gene: CCDC88C

Linked Data

• gnomAD v4: 14-91273720-TGCGCGGGAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91273723_91273731del , CM000676.2:g.91273723_91273731del	GRCh38
NC_000014.8:g.91740067_91740075del , CM000676.1:g.91740067_91740075del	GRCh37
NC_000014.7:g.90809820_90809828del	NCBI36
NG_033118.1:g.149116_149124del
NG_033118.2:g.149116_149124del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5059-76_5059-68del MANE Select	ENSP00000374507.6:n.5059-76_5059-68del
ENST00000331194.8:c.631-76_631-68del	ENSP00000330332.8:n.631-76_631-68del
ENST00000334448.5:n.871-76_871-68del
ENST00000389857.10:c.5059-76_5059-68del	ENSP00000374507.6:n.5059-76_5059-68del
ENST00000556726.5:c.1287-76_1287-68del
NM_001080414.3:c.5059-76_5059-68del	NP_001073883.2:n.5059-76_5059-68del
XM_011536796.1:c.4951-76_4951-68del	XP_011535098.1:n.4951-76_4951-68del
XR_429316.2:n.5334-76_5334-68del
XM_011536796.2:c.4951-76_4951-68del	XP_011535098.1:n.4951-76_4951-68del
XM_017021336.1:c.2140-76_2140-68del	XP_016876825.1:n.2140-76_2140-68del
XR_429316.4:n.5332-76_5332-68del
NM_001080414.4:c.5059-76_5059-68del MANE Select	NP_001073883.2:n.5059-76_5059-68del