Canonical Allele Identifier: CA651343892
Gene: CCDC170 HGNC NCBI

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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618215_151618216insC , CM000668.2:g.151618215_151618216insC GRCh38
NC_000006.11:g.151939350_151939351insC , CM000668.1:g.151939350_151939351insC GRCh37
NC_000006.10:g.151981043_151981044insC NCBI36
NG_021198.1:g.129176_129177insC

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.*68_*69insC MANE Select ENSP00000239374.6:n.*68_*69insC
ENST00000239374.7:c.*68_*69insC ENSP00000239374.6:n.*68_*69insC
NM_025059.3:c.*68_*69insC NP_079335.2:n.*68_*69insC
XM_011536147.1:c.*68_*69insC XP_011534449.1:n.*68_*69insC
XM_011536148.1:c.*68_*69insC XP_011534450.1:n.*68_*69insC
XM_011536147.2:c.*68_*69insC XP_011534449.1:n.*68_*69insC
XM_011536148.2:c.*68_*69insC XP_011534450.1:n.*68_*69insC
NM_025059.4:c.*68_*69insC MANE Select NP_079335.2:n.*68_*69insC
Search 100 bp 5'
Search 100 bp 3'