Canonical Allele Identifier: CA2578772707
Gene: CCDC170 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615598del , CM000668.2:g.151615598del GRCh38
NC_000006.11:g.151936733del , CM000668.1:g.151936733del GRCh37
NC_000006.10:g.151978426del NCBI36
NG_021198.1:g.126559del

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1866del MANE Select ENSP00000239374.6:p.Arg623GlufsTer3
ENST00000239374.7:c.1866del ENSP00000239374.6:p.Arg623GlufsTer3
NM_025059.3:c.1866del NP_079335.2:p.Arg623GlufsTer3
XM_011536147.1:c.1884del XP_011534449.1:p.Arg629GlufsTer3
XM_011536148.1:c.1683del XP_011534450.1:p.Arg562GlufsTer3
XM_011536147.2:c.1884del XP_011534449.1:p.Arg629GlufsTer3
XM_011536148.2:c.1683del XP_011534450.1:p.Arg562GlufsTer3
XR_001743865.1:n.129+1124del
NM_025059.4:c.1866del MANE Select NP_079335.2:p.Arg623GlufsTer3
Search 100 bp 5'
Search 100 bp 3'