Canonical Allele Identifier: CA2713117939
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs68158459

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618628_151618630dup , CM000668.2:g.151618628_151618630dup GRCh38
NC_000006.11:g.151939763_151939765dup , CM000668.1:g.151939763_151939765dup GRCh37
NC_000006.10:g.151981456_151981458dup NCBI36
NG_021198.1:g.129589_129591dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.*481_*483dup MANE Select ENSP00000239374.6:n.*481_*483dup
ENST00000239374.7:c.*481_*483dup ENSP00000239374.6:n.*481_*483dup
NM_025059.3:c.*481_*483dup NP_079335.2:n.*481_*483dup
XM_011536147.1:c.*481_*483dup XP_011534449.1:n.*481_*483dup
XM_011536148.1:c.*481_*483dup XP_011534450.1:n.*481_*483dup
XM_011536147.2:c.*481_*483dup XP_011534449.1:n.*481_*483dup
XM_011536148.2:c.*481_*483dup XP_011534450.1:n.*481_*483dup
NM_025059.4:c.*481_*483dup MANE Select NP_079335.2:n.*481_*483dup