Canonical Allele Identifier: CA366067534
Gene: CCDC170 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615575G>A , CM000668.2:g.151615575G>A GRCh38
NC_000006.11:g.151936710G>A , CM000668.1:g.151936710G>A GRCh37
NC_000006.10:g.151978403G>A NCBI36
NG_021198.1:g.126536G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1843G>A MANE Select ENSP00000239374.6:p.Ala615Thr
ENST00000239374.7:c.1843G>A ENSP00000239374.6:p.Ala615Thr
NM_025059.3:c.1843G>A NP_079335.2:p.Ala615Thr
XM_011536147.1:c.1861G>A XP_011534449.1:p.Ala621Thr
XM_011536148.1:c.1660G>A XP_011534450.1:p.Ala554Thr
XM_011536147.2:c.1861G>A XP_011534449.1:p.Ala621Thr
XM_011536148.2:c.1660G>A XP_011534450.1:p.Ala554Thr
XR_001743865.1:n.129+1146C>T
NM_025059.4:c.1843G>A MANE Select NP_079335.2:p.Ala615Thr