Canonical Allele Identifier: CA651648612
Gene: CCDC170 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151580202_151580203insT , CM000668.2:g.151580202_151580203insT GRCh38
NC_000006.11:g.151901337_151901338insT , CM000668.1:g.151901337_151901338insT GRCh37
NC_000006.10:g.151943030_151943031insT NCBI36
NG_021198.1:g.91163_91164insT

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.1093-5687_1093-5686insT MANE Select ENSP00000239374.6:n.1093-5687_1093-5686in...
ENST00000239374.7:c.1093-5687_1093-5686insT ENSP00000239374.6:n.1093-5687_1093-5686in...
NM_025059.3:c.1093-5687_1093-5686insT NP_079335.2:n.1093-5687_1093-5686insT
XM_011536147.1:c.1111-5687_1111-5686insT XP_011534449.1:n.1111-5687_1111-5686insT
XM_011536148.1:c.1110+6711_1110+6712insT XP_011534450.1:n.1110+6711_1110+6712insT
XM_011536147.2:c.1111-5687_1111-5686insT XP_011534449.1:n.1111-5687_1111-5686insT
XM_011536148.2:c.1110+6711_1110+6712insT XP_011534450.1:n.1110+6711_1110+6712insT
NM_025059.4:c.1093-5687_1093-5686insT MANE Select NP_079335.2:n.1093-5687_1093-5686insT