Canonical Allele Identifier: CA1672964145
Gene: CCDC170 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615364T= , CM000668.2:g.151615364T= GRCh38
NC_000006.11:g.151936499T= , CM000668.1:g.151936499T= GRCh37
NC_000006.10:g.151978192T= NCBI36
NG_021198.1:g.126325T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1711-79T= MANE Select ENSP00000239374.6:n.1711-79T=
ENST00000239374.7:c.1711-79T= ENSP00000239374.6:n.1711-79T=
ENST00000537358.1:n.497-79T=
NM_025059.3:c.1711-79T= NP_079335.2:n.1711-79T=
XM_011536147.1:c.1729-79T= XP_011534449.1:n.1729-79T=
XM_011536148.1:c.1528-79T= XP_011534450.1:n.1528-79T=
XM_011536147.2:c.1729-79T= XP_011534449.1:n.1729-79T=
XM_011536148.2:c.1528-79T= XP_011534450.1:n.1528-79T=
XR_001743865.1:n.129+1357A=
NM_025059.4:c.1711-79T= MANE Select NP_079335.2:n.1711-79T=
Search 100 bp 5'
Search 100 bp 3'