Canonical Allele Identifier: CA1672966336
Gene: CCDC170 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618625_151618628delinsTCTC , CM000668.2:g.151618625_151618628delinsTCTC GRCh38
NC_000006.11:g.151939760_151939763delinsTCTC , CM000668.1:g.151939760_151939763delinsTCTC GRCh37
NC_000006.10:g.151981453_151981456delinsTCTC NCBI36
NG_021198.1:g.129586_129589delinsTCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.*478_*481delinsTCTC MANE Select ENSP00000239374.6:n.*478_*481delinsTCTC
ENST00000239374.7:c.*478_*481delinsTCTC ENSP00000239374.6:n.*478_*481delinsTCTC
NM_025059.3:c.*478_*481delinsTCTC NP_079335.2:n.*478_*481delinsTCTC
XM_011536147.1:c.*478_*481delinsTCTC XP_011534449.1:n.*478_*481delinsTCTC
XM_011536148.1:c.*478_*481delinsTCTC XP_011534450.1:n.*478_*481delinsTCTC
XM_011536147.2:c.*478_*481delinsTCTC XP_011534449.1:n.*478_*481delinsTCTC
XM_011536148.2:c.*478_*481delinsTCTC XP_011534450.1:n.*478_*481delinsTCTC
NM_025059.4:c.*478_*481delinsTCTC MANE Select NP_079335.2:n.*478_*481delinsTCTC
Search 100 bp 5'
Search 100 bp 3'