Canonical Allele Identifier: CA2773571654
Gene: CCDC170 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615645_151615646insCCAAACACACCCAACAC , CM000668.2:g.151615645_151615646insCCAAACACACCCAACAC GRCh38
NC_000006.11:g.151936780_151936781insCCAAACACACCCAACAC , CM000668.1:g.151936780_151936781insCCAAACACACCCAACAC GRCh37
NC_000006.10:g.151978473_151978474insCCAAACACACCCAACAC NCBI36
NG_021198.1:g.126606_126607insCCAAACACACCCAACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1913_1914insCCAAACACACCCAACAC MANE Select ENSP00000239374.6:p.Lys638AsnfsTer30
ENST00000239374.7:c.1913_1914insCCAAACACACCCAACAC ENSP00000239374.6:p.Lys638AsnfsTer30
NM_025059.3:c.1913_1914insCCAAACACACCCAACAC NP_079335.2:p.Lys638AsnfsTer30
XM_011536147.1:c.1931_1932insCCAAACACACCCAACAC XP_011534449.1:p.Lys644AsnfsTer30
XM_011536148.1:c.1730_1731insCCAAACACACCCAACAC XP_011534450.1:p.Lys577AsnfsTer30
XM_011536147.2:c.1931_1932insCCAAACACACCCAACAC XP_011534449.1:p.Lys644AsnfsTer30
XM_011536148.2:c.1730_1731insCCAAACACACCCAACAC XP_011534450.1:p.Lys577AsnfsTer30
XR_001743865.1:n.129+1075_129+1076insGTGTTGGGTGTGTTTGG
NM_025059.4:c.1913_1914insCCAAACACACCCAACAC MANE Select NP_079335.2:p.Lys638AsnfsTer30