Canonical Allele Identifier: CA1672962697
Gene: CCDC170 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615684G= , CM000668.2:g.151615684G= GRCh38
NC_000006.11:g.151936819G= , CM000668.1:g.151936819G= GRCh37
NC_000006.10:g.151978512G= NCBI36
NG_021198.1:g.126645G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1947+5G= MANE Select ENSP00000239374.6:n.1947+5G=
ENST00000239374.7:c.1947+5G= ENSP00000239374.6:n.1947+5G=
NM_025059.3:c.1947+5G= NP_079335.2:n.1947+5G=
XM_011536147.1:c.1965+5G= XP_011534449.1:n.1965+5G=
XM_011536148.1:c.1764+5G= XP_011534450.1:n.1764+5G=
XM_011536147.2:c.1965+5G= XP_011534449.1:n.1965+5G=
XM_011536148.2:c.1764+5G= XP_011534450.1:n.1764+5G=
XR_001743865.1:n.129+1037C=
NM_025059.4:c.1947+5G= MANE Select NP_079335.2:n.1947+5G=
Search 100 bp 5'
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