Canonical Allele Identifier: CA390608139
Gene: CCDC88C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91272739G>T , CM000676.2:g.91272739G>T GRCh38
NC_000014.8:g.91739083G>T , CM000676.1:g.91739083G>T GRCh37
NC_000014.7:g.90808836G>T NCBI36
NG_033118.1:g.150106C>A
NG_033118.2:g.150106C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.5973C>A MANE Select ENSP00000374507.6:p.His1991Gln
ENST00000331194.8:c.1407C>A ENSP00000330332.8:p.His469Gln
ENST00000389857.10:c.5973C>A ENSP00000374507.6:p.His1991Gln
ENST00000556726.5:c.2201C>A
NM_001080414.3:c.5973C>A NP_001073883.2:p.His1991Gln
XM_011536796.1:c.5865C>A XP_011535098.1:p.His1955Gln
XM_011536796.2:c.5865C>A XP_011535098.1:p.His1955Gln
XM_017021336.1:c.3054C>A XP_016876825.1:p.His1018Gln
NM_001080414.4:c.5973C>A MANE Select NP_001073883.2:p.His1991Gln