Canonical Allele Identifier: CA2802580910
Gene: CCDC88C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91272461T>C , CM000676.2:g.91272461T>C GRCh38
NC_000014.8:g.91738805T>C , CM000676.1:g.91738805T>C GRCh37
NC_000014.7:g.90808558T>C NCBI36
NG_033118.1:g.150384A>G
NG_033118.2:g.150384A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.*164A>G MANE Select ENSP00000374507.6:n.*164A>G
ENST00000331194.8:c.*164A>G ENSP00000330332.8:n.*164A>G
ENST00000389857.10:c.*164A>G ENSP00000374507.6:n.*164A>G
ENST00000556726.5:c.2479A>G
NM_001080414.3:c.*164A>G NP_001073883.2:n.*164A>G
XM_011536796.1:c.*164A>G XP_011535098.1:n.*164A>G
XM_011536796.2:c.*164A>G XP_011535098.1:n.*164A>G
XM_017021336.1:c.*164A>G XP_016876825.1:n.*164A>G
NM_001080414.4:c.*164A>G MANE Select NP_001073883.2:n.*164A>G