Canonical Allele Identifier: CA919477246
Gene: CCDC88C HGNC NCBI

Linked Data

dbSNP Id: rs1596007479

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91272534_91272535dup , CM000676.2:g.91272534_91272535dup GRCh38
NC_000014.8:g.91738878_91738879dup , CM000676.1:g.91738878_91738879dup GRCh37
NC_000014.7:g.90808631_90808632dup NCBI36
NG_033118.1:g.150313_150314dup
NG_033118.2:g.150313_150314dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.*93_*94dup MANE Select ENSP00000374507.6:n.*93_*94dup
ENST00000331194.8:c.*93_*94dup ENSP00000330332.8:n.*93_*94dup
ENST00000389857.10:c.*93_*94dup ENSP00000374507.6:n.*93_*94dup
ENST00000556726.5:c.2408_2409dup
NM_001080414.3:c.*93_*94dup NP_001073883.2:n.*93_*94dup
XM_011536796.1:c.*93_*94dup XP_011535098.1:n.*93_*94dup
XM_011536796.2:c.*93_*94dup XP_011535098.1:n.*93_*94dup
XM_017021336.1:c.*93_*94dup XP_016876825.1:n.*93_*94dup
NM_001080414.4:c.*93_*94dup MANE Select NP_001073883.2:n.*93_*94dup