Canonical Allele Identifier: CA2680801639
Gene: CCDC170 HGNC NCBI

Linked Data

gnomAD v4: 6-151618731-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618731C>T , CM000668.2:g.151618731C>T GRCh38
NC_000006.11:g.151939866C>T , CM000668.1:g.151939866C>T GRCh37
NC_000006.10:g.151981559C>T NCBI36
NG_021198.1:g.129692C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.*584C>T MANE Select ENSP00000239374.6:n.*584C>T
ENST00000239374.7:c.*584C>T ENSP00000239374.6:n.*584C>T
NM_025059.3:c.*584C>T NP_079335.2:n.*584C>T
XM_011536147.1:c.*584C>T XP_011534449.1:n.*584C>T
XM_011536148.1:c.*584C>T XP_011534450.1:n.*584C>T
XM_011536147.2:c.*584C>T XP_011534449.1:n.*584C>T
XM_011536148.2:c.*584C>T XP_011534450.1:n.*584C>T
NM_025059.4:c.*584C>T MANE Select NP_079335.2:n.*584C>T
Search 100 bp 5'
Search 100 bp 3'