Canonical Allele Identifier: CA1672965950
Gene: CCDC170 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618193T= , CM000668.2:g.151618193T= GRCh38
NC_000006.11:g.151939328T= , CM000668.1:g.151939328T= GRCh37
NC_000006.10:g.151981021T= NCBI36
NG_021198.1:g.129154T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.*46T= MANE Select ENSP00000239374.6:n.*46T=
ENST00000239374.7:c.*46T= ENSP00000239374.6:n.*46T=
NM_025059.3:c.*46T= NP_079335.2:n.*46T=
XM_011536147.1:c.*46T= XP_011534449.1:n.*46T=
XM_011536148.1:c.*46T= XP_011534450.1:n.*46T=
XM_011536147.2:c.*46T= XP_011534449.1:n.*46T=
XM_011536148.2:c.*46T= XP_011534450.1:n.*46T=
NM_025059.4:c.*46T= MANE Select NP_079335.2:n.*46T=
Search 100 bp 5'
Search 100 bp 3'