Canonical Allele Identifier: CA366067760
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs1776952781

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615597C>A , CM000668.2:g.151615597C>A GRCh38
NC_000006.11:g.151936732C>A , CM000668.1:g.151936732C>A GRCh37
NC_000006.10:g.151978425C>A NCBI36
NG_021198.1:g.126558C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1865C>A MANE Select ENSP00000239374.6:p.Ala622Asp
ENST00000239374.7:c.1865C>A ENSP00000239374.6:p.Ala622Asp
NM_025059.3:c.1865C>A NP_079335.2:p.Ala622Asp
XM_011536147.1:c.1883C>A XP_011534449.1:p.Ala628Asp
XM_011536148.1:c.1682C>A XP_011534450.1:p.Ala561Asp
XM_011536147.2:c.1883C>A XP_011534449.1:p.Ala628Asp
XM_011536148.2:c.1682C>A XP_011534450.1:p.Ala561Asp
XR_001743865.1:n.129+1124G>T
NM_025059.4:c.1865C>A MANE Select NP_079335.2:p.Ala622Asp