Canonical Allele Identifier: CA2680801514
Gene: CCDC170 HGNC NCBI

Linked Data

gnomAD v4: 6-151618627-TCC-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618628_151618629del , CM000668.2:g.151618628_151618629del GRCh38
NC_000006.11:g.151939763_151939764del , CM000668.1:g.151939763_151939764del GRCh37
NC_000006.10:g.151981456_151981457del NCBI36
NG_021198.1:g.129589_129590del

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.*481_*482del MANE Select ENSP00000239374.6:n.*481_*482del
ENST00000239374.7:c.*481_*482del ENSP00000239374.6:n.*481_*482del
NM_025059.3:c.*481_*482del NP_079335.2:n.*481_*482del
XM_011536147.1:c.*481_*482del XP_011534449.1:n.*481_*482del
XM_011536148.1:c.*481_*482del XP_011534450.1:n.*481_*482del
XM_011536147.2:c.*481_*482del XP_011534449.1:n.*481_*482del
XM_011536148.2:c.*481_*482del XP_011534450.1:n.*481_*482del
NM_025059.4:c.*481_*482del MANE Select NP_079335.2:n.*481_*482del
Search 100 bp 5'
Search 100 bp 3'