Canonical Allele Identifier: CA2154899742
Gene: CCDC88C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91272457G= , CM000676.2:g.91272457G= GRCh38
NC_000014.8:g.91738801G= , CM000676.1:g.91738801G= GRCh37
NC_000014.7:g.90808554G= NCBI36
NG_033118.1:g.150388C=
NG_033118.2:g.150388C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.*168C= MANE Select ENSP00000374507.6:n.*168C=
ENST00000331194.8:c.*168C= ENSP00000330332.8:n.*168C=
ENST00000389857.10:c.*168C= ENSP00000374507.6:n.*168C=
ENST00000556726.5:c.2483C=
NM_001080414.3:c.*168C= NP_001073883.2:n.*168C=
XM_011536796.1:c.*168C= XP_011535098.1:n.*168C=
XM_011536796.2:c.*168C= XP_011535098.1:n.*168C=
XM_017021336.1:c.*168C= XP_016876825.1:n.*168C=
NM_001080414.4:c.*168C= MANE Select NP_001073883.2:n.*168C=
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