Canonical Allele Identifier: CA2802581713

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91279424_91279425insAACACACCCAAC , CM000676.2:g.91279424_91279425insAACACACCCAAC	GRCh38
NC_000014.8:g.91745768_91745769insAACACACCCAAC , CM000676.1:g.91745768_91745769insAACACACCCAAC	GRCh37
NC_000014.7:g.90815521_90815522insAACACACCCAAC	NCBI36
NG_033118.1:g.143421_143422insTTGGGTGTGTTG
NG_033118.2:g.143421_143422insTTGGGTGTGTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.4700-118_4700-117insTTGGGTGTGTTG MANE Select	ENSP00000374507.6:n.4700-118_4700-117insTTGGGTGTGTTG
ENST00000331194.8:c.272-118_272-117insTTGGGTGTGTTG	ENSP00000330332.8:n.272-118_272-117insTTGGGTGTGTTG
ENST00000334448.5:n.512-118_512-117insTTGGGTGTGTTG
ENST00000389857.10:c.4700-118_4700-117insTTGGGTGTGTTG	ENSP00000374507.6:n.4700-118_4700-117insTTGGGTGTGTTG
ENST00000556726.5:c.928-118_928-117insTTGGGTGTGTTG
ENST00000557455.1:n.554_555insTTGGGTGTGTTG
NM_001080414.3:c.4700-118_4700-117insTTGGGTGTGTTG	NP_001073883.2:n.4700-118_4700-117insTTGGGTGTGTTG
XM_011536796.1:c.4592-118_4592-117insTTGGGTGTGTTG	XP_011535098.1:n.4592-118_4592-117insTTGGGTGTGTTG
XR_429316.2:n.4975-118_4975-117insTTGGGTGTGTTG
XR_943459.1:n.5465_5466insTTGGGTGTGTTG
XM_011536796.2:c.4592-118_4592-117insTTGGGTGTGTTG	XP_011535098.1:n.4592-118_4592-117insTTGGGTGTGTTG
XM_017021335.2:c.*456_*457insTTGGGTGTGTTG	XP_016876824.1:n.*456_*457insTTGGGTGTGTTG
XM_017021336.1:c.1781-118_1781-117insTTGGGTGTGTTG	XP_016876825.1:n.1781-118_1781-117insTTGGGTGTGTTG
XR_429316.4:n.4973-118_4973-117insTTGGGTGTGTTG
NM_001080414.4:c.4700-118_4700-117insTTGGGTGTGTTG MANE Select	NP_001073883.2:n.4700-118_4700-117insTTGGGTGTGTTG