Canonical Allele Identifier: CA2680801126
Gene: CCDC170 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618131del , CM000668.2:g.151618131del GRCh38
NC_000006.11:g.151939266del , CM000668.1:g.151939266del GRCh37
NC_000006.10:g.151980959del NCBI36
NG_021198.1:g.129092del

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.2132del MANE Select ENSP00000239374.6:p.Leu711TyrfsTer11
ENST00000239374.7:c.2132del ENSP00000239374.6:p.Leu711TyrfsTer11
NM_025059.3:c.2132del NP_079335.2:p.Leu711TyrfsTer11
XM_011536147.1:c.2150del XP_011534449.1:p.Leu717TyrfsTer11
XM_011536148.1:c.1949del XP_011534450.1:p.Leu650TyrfsTer11
XM_011536147.2:c.2150del XP_011534449.1:p.Leu717TyrfsTer11
XM_011536148.2:c.1949del XP_011534450.1:p.Leu650TyrfsTer11
NM_025059.4:c.2132del MANE Select NP_079335.2:p.Leu711TyrfsTer11