Canonical Allele Identifier: CA366066950
Gene: CCDC170 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615503G>A , CM000668.2:g.151615503G>A GRCh38
NC_000006.11:g.151936638G>A , CM000668.1:g.151936638G>A GRCh37
NC_000006.10:g.151978331G>A NCBI36
NG_021198.1:g.126464G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1771G>A MANE Select ENSP00000239374.6:p.Glu591Lys
ENST00000239374.7:c.1771G>A ENSP00000239374.6:p.Glu591Lys
ENST00000537358.1:n.557G>A
NM_025059.3:c.1771G>A NP_079335.2:p.Glu591Lys
XM_011536147.1:c.1789G>A XP_011534449.1:p.Glu597Lys
XM_011536148.1:c.1588G>A XP_011534450.1:p.Glu530Lys
XM_011536147.2:c.1789G>A XP_011534449.1:p.Glu597Lys
XM_011536148.2:c.1588G>A XP_011534450.1:p.Glu530Lys
XR_001743865.1:n.129+1218C>T
NM_025059.4:c.1771G>A MANE Select NP_079335.2:p.Glu591Lys