Canonical Allele Identifier: CA366067755
Gene: CCDC170 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615596G>C , CM000668.2:g.151615596G>C GRCh38
NC_000006.11:g.151936731G>C , CM000668.1:g.151936731G>C GRCh37
NC_000006.10:g.151978424G>C NCBI36
NG_021198.1:g.126557G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1864G>C MANE Select ENSP00000239374.6:p.Ala622Pro
ENST00000239374.7:c.1864G>C ENSP00000239374.6:p.Ala622Pro
NM_025059.3:c.1864G>C NP_079335.2:p.Ala622Pro
XM_011536147.1:c.1882G>C XP_011534449.1:p.Ala628Pro
XM_011536148.1:c.1681G>C XP_011534450.1:p.Ala561Pro
XM_011536147.2:c.1882G>C XP_011534449.1:p.Ala628Pro
XM_011536148.2:c.1681G>C XP_011534450.1:p.Ala561Pro
XR_001743865.1:n.129+1125C>G
NM_025059.4:c.1864G>C MANE Select NP_079335.2:p.Ala622Pro