Canonical Allele Identifier: CA2575602905

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91279151_91279152insA , CM000676.2:g.91279151_91279152insA	GRCh38
NC_000014.8:g.91745495_91745496insA , CM000676.1:g.91745495_91745496insA	GRCh37
NC_000014.7:g.90815248_90815249insA	NCBI36
NG_033118.1:g.143693_143694insT
NG_033118.2:g.143693_143694insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.4768+86_4768+87insT MANE Select	ENSP00000374507.6:n.4768+86_4768+87insT
ENST00000331194.8:c.340+86_340+87insT	ENSP00000330332.8:n.340+86_340+87insT
ENST00000334448.5:n.580+86_580+87insT
ENST00000389857.10:c.4768+86_4768+87insT	ENSP00000374507.6:n.4768+86_4768+87insT
ENST00000556726.5:c.996+86_996+87insT
ENST00000557455.1:n.740+86_740+87insT
NM_001080414.3:c.4768+86_4768+87insT	NP_001073883.2:n.4768+86_4768+87insT
XM_011536796.1:c.4660+86_4660+87insT	XP_011535098.1:n.4660+86_4660+87insT
XR_429316.2:n.5043+86_5043+87insT
XM_011536796.2:c.4660+86_4660+87insT	XP_011535098.1:n.4660+86_4660+87insT
XM_017021336.1:c.1849+86_1849+87insT	XP_016876825.1:n.1849+86_1849+87insT
XR_429316.4:n.5041+86_5041+87insT
NM_001080414.4:c.4768+86_4768+87insT MANE Select	NP_001073883.2:n.4768+86_4768+87insT