Canonical Allele Identifier: CA1672966344
Gene: CCDC170 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618628C= , CM000668.2:g.151618628C= GRCh38
NC_000006.11:g.151939763C= , CM000668.1:g.151939763C= GRCh37
NC_000006.10:g.151981456C= NCBI36
NG_021198.1:g.129589C=

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.*481C= MANE Select ENSP00000239374.6:n.*481C=
ENST00000239374.7:c.*481C= ENSP00000239374.6:n.*481C=
NM_025059.3:c.*481C= NP_079335.2:n.*481C=
XM_011536147.1:c.*481C= XP_011534449.1:n.*481C=
XM_011536148.1:c.*481C= XP_011534450.1:n.*481C=
XM_011536147.2:c.*481C= XP_011534449.1:n.*481C=
XM_011536148.2:c.*481C= XP_011534450.1:n.*481C=
NM_025059.4:c.*481C= MANE Select NP_079335.2:n.*481C=