Canonical Allele Identifier: CA487540755
Gene: CCDC88C HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.91745645G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91279301G>T , CM000676.2:g.91279301G>T GRCh38
NC_000014.8:g.91745645G>T , CM000676.1:g.91745645G>T GRCh37
NC_000014.7:g.90815398G>T NCBI36
NG_033118.1:g.143544C>A
NG_033118.2:g.143544C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000389857.11:c.4705C>A MANE Select ENSP00000374507.6:p.Arg1569=
ENST00000331194.8:c.277C>A ENSP00000330332.8:p.Arg93=
ENST00000334448.5:n.517C>A
ENST00000389857.10:c.4705C>A ENSP00000374507.6:p.Arg1569=
ENST00000556726.5:c.933C>A
ENST00000557455.1:n.677C>A
NM_001080414.3:c.4705C>A NP_001073883.2:p.Arg1569=
XM_011536796.1:c.4597C>A XP_011535098.1:p.Arg1533=
XR_429316.2:n.4980C>A
XM_011536796.2:c.4597C>A XP_011535098.1:p.Arg1533=
XM_017021336.1:c.1786C>A XP_016876825.1:p.Arg596=
XR_429316.4:n.4978C>A
NM_001080414.4:c.4705C>A MANE Select NP_001073883.2:p.Arg1569=