Canonical Allele Identifier: CA2154902828
Gene: CCDC88C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91273632C= , CM000676.2:g.91273632C= GRCh38
NC_000014.8:g.91739976C= , CM000676.1:g.91739976C= GRCh37
NC_000014.7:g.90809729C= NCBI36
NG_033118.1:g.149213G=
NG_033118.2:g.149213G=

Transcript Alleles

HGVS Amino-acid change
ENST00000389857.11:c.5080G= MANE Select ENSP00000374507.6:p.Asp1694=
ENST00000331194.8:c.652G= ENSP00000330332.8:p.Asp218=
ENST00000334448.5:n.892G=
ENST00000389857.10:c.5080G= ENSP00000374507.6:p.Asp1694=
ENST00000556726.5:c.1308G=
NM_001080414.3:c.5080G= NP_001073883.2:p.Asp1694=
XM_011536796.1:c.4972G= XP_011535098.1:p.Asp1658=
XR_429316.2:n.5355G=
XM_011536796.2:c.4972G= XP_011535098.1:p.Asp1658=
XM_017021336.1:c.2161G= XP_016876825.1:p.Asp721=
XR_429316.4:n.5353G=
NM_001080414.4:c.5080G= MANE Select NP_001073883.2:p.Asp1694=