Canonical Allele Identifier: CA1672966422
Gene: CCDC170 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618713C= , CM000668.2:g.151618713C= GRCh38
NC_000006.11:g.151939848C= , CM000668.1:g.151939848C= GRCh37
NC_000006.10:g.151981541C= NCBI36
NG_021198.1:g.129674C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.*566C= MANE Select ENSP00000239374.6:n.*566C=
ENST00000239374.7:c.*566C= ENSP00000239374.6:n.*566C=
NM_025059.3:c.*566C= NP_079335.2:n.*566C=
XM_011536147.1:c.*566C= XP_011534449.1:n.*566C=
XM_011536148.1:c.*566C= XP_011534450.1:n.*566C=
XM_011536147.2:c.*566C= XP_011534449.1:n.*566C=
XM_011536148.2:c.*566C= XP_011534450.1:n.*566C=
NM_025059.4:c.*566C= MANE Select NP_079335.2:n.*566C=