Canonical Allele Identifier: CA2154899797
Gene: CCDC88C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91272509A= , CM000676.2:g.91272509A= GRCh38
NC_000014.8:g.91738853A= , CM000676.1:g.91738853A= GRCh37
NC_000014.7:g.90808606A= NCBI36
NG_033118.1:g.150336T=
NG_033118.2:g.150336T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.*116T= MANE Select ENSP00000374507.6:n.*116T=
ENST00000331194.8:c.*116T= ENSP00000330332.8:n.*116T=
ENST00000389857.10:c.*116T= ENSP00000374507.6:n.*116T=
ENST00000556726.5:c.2431T=
NM_001080414.3:c.*116T= NP_001073883.2:n.*116T=
XM_011536796.1:c.*116T= XP_011535098.1:n.*116T=
XM_011536796.2:c.*116T= XP_011535098.1:n.*116T=
XM_017021336.1:c.*116T= XP_016876825.1:n.*116T=
NM_001080414.4:c.*116T= MANE Select NP_001073883.2:n.*116T=
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