Canonical Allele Identifier: CA2680801504
Gene: CCDC170 HGNC NCBI

Linked Data

gnomAD v4: 6-151618620-C-CCCTGT
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618621_151618622insCTGTC , CM000668.2:g.151618621_151618622insCTGTC GRCh38
NC_000006.11:g.151939756_151939757insCTGTC , CM000668.1:g.151939756_151939757insCTGTC GRCh37
NC_000006.10:g.151981449_151981450insCTGTC NCBI36
NG_021198.1:g.129582_129583insCTGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.*474_*475insCTGTC MANE Select ENSP00000239374.6:n.*474_*475insCTGTC
ENST00000239374.7:c.*474_*475insCTGTC ENSP00000239374.6:n.*474_*475insCTGTC
NM_025059.3:c.*474_*475insCTGTC NP_079335.2:n.*474_*475insCTGTC
XM_011536147.1:c.*474_*475insCTGTC XP_011534449.1:n.*474_*475insCTGTC
XM_011536148.1:c.*474_*475insCTGTC XP_011534450.1:n.*474_*475insCTGTC
XM_011536147.2:c.*474_*475insCTGTC XP_011534449.1:n.*474_*475insCTGTC
XM_011536148.2:c.*474_*475insCTGTC XP_011534450.1:n.*474_*475insCTGTC
NM_025059.4:c.*474_*475insCTGTC MANE Select NP_079335.2:n.*474_*475insCTGTC
Search 100 bp 5'
Search 100 bp 3'