Canonical Allele Identifier: CA651343899
Gene: CCDC170 HGNC NCBI

Linked Data

COSMIC: COSN17038321
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618727_151618728insT , CM000668.2:g.151618727_151618728insT GRCh38
NC_000006.11:g.151939862_151939863insT , CM000668.1:g.151939862_151939863insT GRCh37
NC_000006.10:g.151981555_151981556insT NCBI36
NG_021198.1:g.129688_129689insT

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.*580_*581insT MANE Select ENSP00000239374.6:n.*580_*581insT
ENST00000239374.7:c.*580_*581insT ENSP00000239374.6:n.*580_*581insT
NM_025059.3:c.*580_*581insT NP_079335.2:n.*580_*581insT
XM_011536147.1:c.*580_*581insT XP_011534449.1:n.*580_*581insT
XM_011536148.1:c.*580_*581insT XP_011534450.1:n.*580_*581insT
XM_011536147.2:c.*580_*581insT XP_011534449.1:n.*580_*581insT
XM_011536148.2:c.*580_*581insT XP_011534450.1:n.*580_*581insT
NM_025059.4:c.*580_*581insT MANE Select NP_079335.2:n.*580_*581insT
Search 100 bp 5'
Search 100 bp 3'