Canonical Allele Identifier: CA2802581708
Gene: CCDC88C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91279215del , CM000676.2:g.91279215del GRCh38
NC_000014.8:g.91745559del , CM000676.1:g.91745559del GRCh37
NC_000014.7:g.90815312del NCBI36
NG_033118.1:g.143630del
NG_033118.2:g.143630del

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.4768+23del MANE Select ENSP00000374507.6:n.4768+23del
ENST00000331194.8:c.340+23del ENSP00000330332.8:n.340+23del
ENST00000334448.5:n.580+23del
ENST00000389857.10:c.4768+23del ENSP00000374507.6:n.4768+23del
ENST00000556726.5:c.996+23del
ENST00000557455.1:n.740+23del
NM_001080414.3:c.4768+23del NP_001073883.2:n.4768+23del
XM_011536796.1:c.4660+23del XP_011535098.1:n.4660+23del
XR_429316.2:n.5043+23del
XM_011536796.2:c.4660+23del XP_011535098.1:n.4660+23del
XM_017021336.1:c.1849+23del XP_016876825.1:n.1849+23del
XR_429316.4:n.5041+23del
NM_001080414.4:c.4768+23del MANE Select NP_001073883.2:n.4768+23del