Canonical Allele Identifier: CA1672966013
Gene: CCDC170 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618235_151618236delinsGT , CM000668.2:g.151618235_151618236delinsGT GRCh38
NC_000006.11:g.151939370_151939371delinsGT , CM000668.1:g.151939370_151939371delinsGT GRCh37
NC_000006.10:g.151981063_151981064delinsGT NCBI36
NG_021198.1:g.129196_129197delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.*88_*89delinsGT MANE Select ENSP00000239374.6:n.*88_*89delinsGT
ENST00000239374.7:c.*88_*89delinsGT ENSP00000239374.6:n.*88_*89delinsGT
NM_025059.3:c.*88_*89delinsGT NP_079335.2:n.*88_*89delinsGT
XM_011536147.1:c.*88_*89delinsGT XP_011534449.1:n.*88_*89delinsGT
XM_011536148.1:c.*88_*89delinsGT XP_011534450.1:n.*88_*89delinsGT
XM_011536147.2:c.*88_*89delinsGT XP_011534449.1:n.*88_*89delinsGT
XM_011536148.2:c.*88_*89delinsGT XP_011534450.1:n.*88_*89delinsGT
NM_025059.4:c.*88_*89delinsGT MANE Select NP_079335.2:n.*88_*89delinsGT
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