Canonical Allele Identifier: CA1672962830
Gene: CCDC170 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615754T= , CM000668.2:g.151615754T= GRCh38
NC_000006.11:g.151936889T= , CM000668.1:g.151936889T= GRCh37
NC_000006.10:g.151978582T= NCBI36
NG_021198.1:g.126715T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1947+75T= MANE Select ENSP00000239374.6:n.1947+75T=
ENST00000239374.7:c.1947+75T= ENSP00000239374.6:n.1947+75T=
NM_025059.3:c.1947+75T= NP_079335.2:n.1947+75T=
XM_011536147.1:c.1965+75T= XP_011534449.1:n.1965+75T=
XM_011536148.1:c.1764+75T= XP_011534450.1:n.1764+75T=
XM_011536147.2:c.1965+75T= XP_011534449.1:n.1965+75T=
XM_011536148.2:c.1764+75T= XP_011534450.1:n.1764+75T=
XR_001743865.1:n.129+967A=
NM_025059.4:c.1947+75T= MANE Select NP_079335.2:n.1947+75T=
Search 100 bp 5'
Search 100 bp 3'