Canonical Allele Identifier: CA1672965998
Gene: CCDC170 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618216T= , CM000668.2:g.151618216T= GRCh38
NC_000006.11:g.151939351T= , CM000668.1:g.151939351T= GRCh37
NC_000006.10:g.151981044T= NCBI36
NG_021198.1:g.129177T=

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.*69T= MANE Select ENSP00000239374.6:n.*69T=
ENST00000239374.7:c.*69T= ENSP00000239374.6:n.*69T=
NM_025059.3:c.*69T= NP_079335.2:n.*69T=
XM_011536147.1:c.*69T= XP_011534449.1:n.*69T=
XM_011536148.1:c.*69T= XP_011534450.1:n.*69T=
XM_011536147.2:c.*69T= XP_011534449.1:n.*69T=
XM_011536148.2:c.*69T= XP_011534450.1:n.*69T=
NM_025059.4:c.*69T= MANE Select NP_079335.2:n.*69T=