Canonical Allele Identifier: CA2154909482
Gene: CCDC88C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91279300C= , CM000676.2:g.91279300C= GRCh38
NC_000014.8:g.91745644C= , CM000676.1:g.91745644C= GRCh37
NC_000014.7:g.90815397C= NCBI36
NG_033118.1:g.143545G=
NG_033118.2:g.143545G=

Transcript Alleles

HGVS Amino-acid change
ENST00000389857.11:c.4706G= MANE Select ENSP00000374507.6:p.Arg1569=
ENST00000331194.8:c.278G= ENSP00000330332.8:p.Arg93=
ENST00000334448.5:n.518G=
ENST00000389857.10:c.4706G= ENSP00000374507.6:p.Arg1569=
ENST00000556726.5:c.934G=
ENST00000557455.1:n.678G=
NM_001080414.3:c.4706G= NP_001073883.2:p.Arg1569=
XM_011536796.1:c.4598G= XP_011535098.1:p.Arg1533=
XR_429316.2:n.4981G=
XM_011536796.2:c.4598G= XP_011535098.1:p.Arg1533=
XM_017021336.1:c.1787G= XP_016876825.1:p.Arg596=
XR_429316.4:n.4979G=
NM_001080414.4:c.4706G= MANE Select NP_001073883.2:p.Arg1569=