Canonical Allele Identifier: CA1672966432
Gene: CCDC170 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618727C= , CM000668.2:g.151618727C= GRCh38
NC_000006.11:g.151939862C= , CM000668.1:g.151939862C= GRCh37
NC_000006.10:g.151981555C= NCBI36
NG_021198.1:g.129688C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.*580C= MANE Select ENSP00000239374.6:n.*580C=
ENST00000239374.7:c.*580C= ENSP00000239374.6:n.*580C=
NM_025059.3:c.*580C= NP_079335.2:n.*580C=
XM_011536147.1:c.*580C= XP_011534449.1:n.*580C=
XM_011536148.1:c.*580C= XP_011534450.1:n.*580C=
XM_011536147.2:c.*580C= XP_011534449.1:n.*580C=
XM_011536148.2:c.*580C= XP_011534450.1:n.*580C=
NM_025059.4:c.*580C= MANE Select NP_079335.2:n.*580C=