Canonical Allele Identifier: CA2154899706
Gene: CCDC88C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91272429T= , CM000676.2:g.91272429T= GRCh38
NC_000014.8:g.91738773T= , CM000676.1:g.91738773T= GRCh37
NC_000014.7:g.90808526T= NCBI36
NG_033118.1:g.150416A=
NG_033118.2:g.150416A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389857.11:c.*196A= MANE Select ENSP00000374507.6:n.*196A=
ENST00000331194.8:c.*196A= ENSP00000330332.8:n.*196A=
ENST00000389857.10:c.*196A= ENSP00000374507.6:n.*196A=
ENST00000556726.5:c.2511A=
NM_001080414.3:c.*196A= NP_001073883.2:n.*196A=
XM_011536796.1:c.*196A= XP_011535098.1:n.*196A=
XM_011536796.2:c.*196A= XP_011535098.1:n.*196A=
XM_017021336.1:c.*196A= XP_016876825.1:n.*196A=
NM_001080414.4:c.*196A= MANE Select NP_001073883.2:n.*196A=
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