Canonical Allele Identifier: CA2154900414
Gene: CCDC88C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91272783_91272784delinsGC , CM000676.2:g.91272783_91272784delinsGC GRCh38
NC_000014.8:g.91739127_91739128delinsGC , CM000676.1:g.91739127_91739128delinsGC GRCh37
NC_000014.7:g.90808880_90808881delinsGC NCBI36
NG_033118.1:g.150061_150062delinsGC
NG_033118.2:g.150061_150062delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.5928_5929delinsGC MANE Select ENSP00000374507.6:p.Gly1976=
ENST00000331194.8:c.1362_1363delinsGC ENSP00000330332.8:p.Gly454=
ENST00000389857.10:c.5928_5929delinsGC ENSP00000374507.6:p.Gly1976=
ENST00000556726.5:c.2156_2157delinsGC
NM_001080414.3:c.5928_5929delinsGC NP_001073883.2:p.Gly1976=
XM_011536796.1:c.5820_5821delinsGC XP_011535098.1:p.Gly1940=
XM_011536796.2:c.5820_5821delinsGC XP_011535098.1:p.Gly1940=
XM_017021336.1:c.3009_3010delinsGC XP_016876825.1:p.Gly1003=
NM_001080414.4:c.5928_5929delinsGC MANE Select NP_001073883.2:p.Gly1976=