Canonical Allele Identifier: CA1672961480

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151612017_151612020delinsTTTC , CM000668.2:g.151612017_151612020delinsTTTC	GRCh38
NC_000006.11:g.151933152_151933155delinsTTTC , CM000668.1:g.151933152_151933155delinsTTTC	GRCh37
NC_000006.10:g.151974845_151974848delinsTTTC	NCBI36
NG_021198.1:g.122978_122981delinsTTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000239374.8:c.1711-3426_1711-3423delinsTTTC MANE Select	ENSP00000239374.6:n.1711-3426_1711-3423delinsTTTC
ENST00000239374.7:c.1711-3426_1711-3423delinsTTTC	ENSP00000239374.6:n.1711-3426_1711-3423delinsTTTC
ENST00000537358.1:n.497-3426_497-3423delinsTTTC
NM_025059.3:c.1711-3426_1711-3423delinsTTTC	NP_079335.2:n.1711-3426_1711-3423delinsTTTC
XM_011536147.1:c.1729-3426_1729-3423delinsTTTC	XP_011534449.1:n.1729-3426_1729-3423delinsTTTC
XM_011536148.1:c.1528-3426_1528-3423delinsTTTC	XP_011534450.1:n.1528-3426_1528-3423delinsTTTC
XM_011536147.2:c.1729-3426_1729-3423delinsTTTC	XP_011534449.1:n.1729-3426_1729-3423delinsTTTC
XM_011536148.2:c.1528-3426_1528-3423delinsTTTC	XP_011534450.1:n.1528-3426_1528-3423delinsTTTC
XR_001743865.1:n.130-748_130-745delinsGAAA
NM_025059.4:c.1711-3426_1711-3423delinsTTTC MANE Select	NP_079335.2:n.1711-3426_1711-3423delinsTTTC