Canonical Allele Identifier: CA4051987
Gene: CCDC170 HGNC NCBI

Linked Data

ClinVar Variation Id: 2354677
ClinVar RCV Id: RCV004195162
dbSNP Id: rs371502185

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615572G>A , CM000668.2:g.151615572G>A GRCh38
NC_000006.11:g.151936707G>A , CM000668.1:g.151936707G>A GRCh37
NC_000006.10:g.151978400G>A NCBI36
NG_021198.1:g.126533G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1840G>A MANE Select ENSP00000239374.6:p.Glu614Lys
ENST00000239374.7:c.1840G>A ENSP00000239374.6:p.Glu614Lys
NM_025059.3:c.1840G>A NP_079335.2:p.Glu614Lys
XM_011536147.1:c.1858G>A XP_011534449.1:p.Glu620Lys
XM_011536148.1:c.1657G>A XP_011534450.1:p.Glu553Lys
XM_011536147.2:c.1858G>A XP_011534449.1:p.Glu620Lys
XM_011536148.2:c.1657G>A XP_011534450.1:p.Glu553Lys
XR_001743865.1:n.129+1149C>T
NM_025059.4:c.1840G>A MANE Select NP_079335.2:p.Glu614Lys