Canonical Allele Identifier: CA150138001
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs9479055

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526832C>A , CM000668.2:g.151526832C>A GRCh38
NC_000006.11:g.151847967C>A , CM000668.1:g.151847967C>A GRCh37
NC_000006.10:g.151889660C>A NCBI36
NG_021198.1:g.37793C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.58-9486C>A MANE Select ENSP00000239374.6:p.=
ENST00000239374.7:c.58-9486C>A ENSP00000239374.6:p.=
NM_025059.3:c.58-9486C>A NP_079335.2:p.=
NM_025059.4:c.58-9486C>A MANE Select NP_079335.2:p.=