Canonical Allele Identifier: CA2154902820
Gene: CCDC88C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91273631T= , CM000676.2:g.91273631T= GRCh38
NC_000014.8:g.91739975T= , CM000676.1:g.91739975T= GRCh37
NC_000014.7:g.90809728T= NCBI36
NG_033118.1:g.149214A=
NG_033118.2:g.149214A=

Transcript Alleles

HGVS Amino-acid change
ENST00000389857.11:c.5081A= MANE Select ENSP00000374507.6:p.Asp1694=
ENST00000331194.8:c.653A= ENSP00000330332.8:p.Asp218=
ENST00000334448.5:n.893A=
ENST00000389857.10:c.5081A= ENSP00000374507.6:p.Asp1694=
ENST00000556726.5:c.1309A=
NM_001080414.3:c.5081A= NP_001073883.2:p.Asp1694=
XM_011536796.1:c.4973A= XP_011535098.1:p.Asp1658=
XR_429316.2:n.5356A=
XM_011536796.2:c.4973A= XP_011535098.1:p.Asp1658=
XM_017021336.1:c.2162A= XP_016876825.1:p.Asp721=
XR_429316.4:n.5354A=
NM_001080414.4:c.5081A= MANE Select NP_001073883.2:p.Asp1694=