Canonical Allele Identifier: CA917888784
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs1554227694

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618627_151618628dup , CM000668.2:g.151618627_151618628dup GRCh38
NC_000006.11:g.151939762_151939763dup , CM000668.1:g.151939762_151939763dup GRCh37
NC_000006.10:g.151981455_151981456dup NCBI36
NG_021198.1:g.129588_129589dup

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.*480_*481dup MANE Select ENSP00000239374.6:n.*480_*481dup
ENST00000239374.7:c.*480_*481dup ENSP00000239374.6:n.*480_*481dup
NM_025059.3:c.*480_*481dup NP_079335.2:n.*480_*481dup
XM_011536147.1:c.*480_*481dup XP_011534449.1:n.*480_*481dup
XM_011536148.1:c.*480_*481dup XP_011534450.1:n.*480_*481dup
XM_011536147.2:c.*480_*481dup XP_011534449.1:n.*480_*481dup
XM_011536148.2:c.*480_*481dup XP_011534450.1:n.*480_*481dup
NM_025059.4:c.*480_*481dup MANE Select NP_079335.2:n.*480_*481dup