Canonical Allele Identifier: CA1672946977
Gene: CCDC170 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151580215T= , CM000668.2:g.151580215T= GRCh38
NC_000006.11:g.151901350T= , CM000668.1:g.151901350T= GRCh37
NC_000006.10:g.151943043T= NCBI36
NG_021198.1:g.91176T=

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.1093-5674T= MANE Select ENSP00000239374.6:n.1093-5674T=
ENST00000239374.7:c.1093-5674T= ENSP00000239374.6:n.1093-5674T=
NM_025059.3:c.1093-5674T= NP_079335.2:n.1093-5674T=
XM_011536147.1:c.1111-5674T= XP_011534449.1:n.1111-5674T=
XM_011536148.1:c.1110+6724T= XP_011534450.1:n.1110+6724T=
XM_011536147.2:c.1111-5674T= XP_011534449.1:n.1111-5674T=
XM_011536148.2:c.1110+6724T= XP_011534450.1:n.1110+6724T=
NM_025059.4:c.1093-5674T= MANE Select NP_079335.2:n.1093-5674T=
Search 100 bp 5'
Search 100 bp 3'