Canonical Allele Identifier: CA1672947021
Gene: CCDC170 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151580304_151580305delinsCT , CM000668.2:g.151580304_151580305delinsCT GRCh38
NC_000006.11:g.151901439_151901440delinsCT , CM000668.1:g.151901439_151901440delinsCT GRCh37
NC_000006.10:g.151943132_151943133delinsCT NCBI36
NG_021198.1:g.91265_91266delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.1093-5585_1093-5584delinsCT MANE Select ENSP00000239374.6:n.1093-5585_1093-5584de...
ENST00000239374.7:c.1093-5585_1093-5584delinsCT ENSP00000239374.6:n.1093-5585_1093-5584de...
NM_025059.3:c.1093-5585_1093-5584delinsCT NP_079335.2:n.1093-5585_1093-5584delinsCT...
XM_011536147.1:c.1111-5585_1111-5584delinsCT XP_011534449.1:n.1111-5585_1111-5584delin...
XM_011536148.1:c.1110+6813_1110+6814delinsCT XP_011534450.1:n.1110+6813_1110+6814delin...
XM_011536147.2:c.1111-5585_1111-5584delinsCT XP_011534449.1:n.1111-5585_1111-5584delin...
XM_011536148.2:c.1110+6813_1110+6814delinsCT XP_011534450.1:n.1110+6813_1110+6814delin...
NM_025059.4:c.1093-5585_1093-5584delinsCT MANE Select NP_079335.2:n.1093-5585_1093-5584delinsCT...