Canonical Allele Identifier: CA1672946950
Gene: CCDC170 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151580165_151580175delinsGACTATGGCTA , CM000668.2:g.151580165_151580175delinsGACTATGGCTA GRCh38
NC_000006.11:g.151901300_151901310delinsGACTATGGCTA , CM000668.1:g.151901300_151901310delinsGACTATGGCTA GRCh37
NC_000006.10:g.151942993_151943003delinsGACTATGGCTA NCBI36
NG_021198.1:g.91126_91136delinsGACTATGGCTA

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.1093-5724_1093-5714delinsGACTATGGCTA MANE Select ENSP00000239374.6:n.1093-5724_1093-5714de...
ENST00000239374.7:c.1093-5724_1093-5714delinsGACTATGGCTA ENSP00000239374.6:n.1093-5724_1093-5714de...
NM_025059.3:c.1093-5724_1093-5714delinsGACTATGGCTA NP_079335.2:n.1093-5724_1093-5714delinsGA...
XM_011536147.1:c.1111-5724_1111-5714delinsGACTATGGCTA XP_011534449.1:n.1111-5724_1111-5714delin...
XM_011536148.1:c.1110+6674_1110+6684delinsGACTATGGCTA XP_011534450.1:n.1110+6674_1110+6684delin...
XM_011536147.2:c.1111-5724_1111-5714delinsGACTATGGCTA XP_011534449.1:n.1111-5724_1111-5714delin...
XM_011536148.2:c.1110+6674_1110+6684delinsGACTATGGCTA XP_011534450.1:n.1110+6674_1110+6684delin...
NM_025059.4:c.1093-5724_1093-5714delinsGACTATGGCTA MANE Select NP_079335.2:n.1093-5724_1093-5714delinsGA...